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Medical Trials, Clinical Trials, Drug Trials, Medical Research, Clinical Research Opportunities for Study Participants in

473 studies recruit in and from this area



Study 1599 :Healthy Right Handed Non Smoking Males Aged 18-35yrs
London


Type of StudyWe need volunteers to come to the Institute of Psychiatry on 3 occasions (each separated by 14 days) from 10am – 4:30pm. On each visit you will be asked to:

- Ingest a low dose of antipsychotic medication or a placebo (may cause

restlessness, agitation, nausea or short-lived 'dystonic reaction' involving spasm

of certain muscle groups)

- provide a blood sample equivalent to 3.5 teaspoons

- provide cheek swabs and saliva samples

- have an MRI scan whilst completing some computer tasks

- complete questionnaires (rate mood & provide socio-demographic information)

Aim of StudyAs part of a larger study investigating genetics and psychiatric illnesses, we are trying to find out how medications called haloperidol and aripiprazole (used to treat various types of mental illness such as psychosis) affect the brain. Exploring these effects in healthy individuals enables us to better understand the role of these drugs in the treatment of mental health.

Inclusion Criteria Healthy males

- Caucasian & first language English

- Completing a degree or have already graduated

- Aged 18-35yrs

- Right handed

- Non-smokers & non-recreational drug users

- Volunteers available in July, August OR September.

Area South London (Camberwell)
Duration We need volunteers to come to the Institute of Psychiatry on 3 occasions (each separated by 14 days) from 10am – 4:30pm.
Reimbursement TRAVEL EXPENSES AND YOUR TIME WILL BE REIMBURSED. Lunch is provided and brain images can be provided on request.
Other InfoThe Joint South London and Maudsley and The Institute of Psychiatry NHS Research Ethics Committee reference: 05/Q0706/158 (135/05).

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HEALTH ZONE NEWS LETTER ABOVE ABOUT MRI SCANS

Study 1598 : Studies for dry eye sufferers
London


Type of Study Studies testing the efficiency of eye drops in relieving DRY EYE symptoms
Aim of StudyTesting the performance of eye drops in relieving DRY EYE symptoms
Inclusion Criteria Male and Female
Participants 18 years above.
Contact lens wearers or Non Contact Lens Wearers who suffer from DRY EYE.
People with medical conditions and who are on medications can apply.
NO Doctors registration required.
Exclusion Criteria The medications or medical conditions must not affect the eye.
Area Volunteers from London area only.
Duration Variable.
Reimbursement IF YOU ARE FOUND TO BE SUITABLE, all products and services will be provided free of charge for the duration of the trial in return for your participation and you may receive compensation for your time & travel.
Other InfoYOU TUBE ABOVE - WILL DOWNING - NICE SAX
NotesAPPLY BELOW

Study 1597 :Contact lens Studies.
London


Study Added: 23/05/2008
Type of Study Contact lens studies for CURRENT contact lens wearers
Inclusion Criteria Male and Female participants
18 years above.
Spectacle wearers.
NO Doctors registration required.
People with medical conditions and who are on medications can apply.
Exclusion Criteria No systemic disease or medication or allergies which may interfere with contact lens wear
Area Volunteers from LONDON area only
Duration Variable
Reimbursement IF YOU ARE FOUND TO BE SUITABLE, all contact lenses and services will be provided free of charge for the duration of the trial in return for your participation and you may receive compensation for your time & travel.
Other InfoYOU TUBE ABOVE - PM DAWN - SET ADRIFT ON MEMORY BLISS
NotesAPPLY BELOW

Study 1596 :Contact lens Studies. Do you want to try contact lenses?
London


Study Added: 23/05/2008
Type of Study Contact lens studies for spectacles wearers
Inclusion Criteria Male and Female participants
18 years above.
Spectacle wearers.
NO Doctors registration required.
People with medical conditions and who are on medications can apply.
Exclusion Criteria No systemic disease or medication or allergies which may interfere with contact lens wear
Area Volunteers from LONDON area only
Duration Variable
Reimbursement IF YOU ARE FOUND TO BE SUITABLE, all contact lenses and services will be provided free of charge for the duration of the trial in return for your participation and you may receive compensation for your time & travel.
Other InfoYOU TUBE ABOVE - JON SECADA - JUST ANOTHER DAY
NotesAPPLY BELOW

Study 1584 :Photobiology Study For Males & Females Aged 20 - 60
Manchester


Study Added: 02/07/2008
Type of StudyUptake of Omega-3 Fatty Acids into the Skin

study will involve application of creams containing omega-3 fatty acids to areas of your upper buttock skin. In addition small areas of your buttock skin will be exposed to ultraviolet light and a total of 6 skin samples will then be taken from these areas on your buttock.
Aim of StudyThis is a research project aimed at understanding the biological processes involved in sun damage to human skin and how omega-3 fatty acids can help protect against sunburn.
Inclusion Criteria Participants must be healthy adults between 20 and 60 years of age;
Participants must be white Caucasian.
Exclusion Criteria People who have sunbathed (artificial or sunlight) in the last 3 months;
People taking photoactive, anti-inflammatory or immunosuppressive drugs;
People with a history of photosensitivity disorders;
People with a history of skin cancer;
People who are hospitalised, and/or deprived of freedom or who are under legal guardianship;
People who are pregnant;
People who smoke;
People who are prone to keloid scarring.
Area Salford, Lancashire
Duration If you are eligible to take part in the study you will be asked to visit the clinic 3 times over a period of 5 days
Reimbursement In view of the time and inconvenience involved in taking part in the study, you will receive a reimbursement of £15 per biopsy and £10 per visit.
Other InfoSEE REAL INFORMED CONSENT NOTES ABOVE

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Study 1476 :Generalized Anxiety Disorder
Pennsylvania


 
Study Added: 11/01/2008
Type of StudyCRI Worldwide is conducting a research study of an investigational medication for anxiety sufferers.
Aim of StudyThe purpose of this study is to look at the Efficacy and Safety of the medication compared to a placebo.
Inclusion CriteriaTo qualify you must be between the ages of 18 and 65 and currently taking medication to treat your anxiety.
Exclusion CriteriaParticipating in another research study in the last 30 days.
Any type of seizure disorder.
AreaNortheast Philadelphia
DurationUp to 12 Weeks
ReimbursementParticipants who qualify and enroll in the study will receive $30.00 per visit.
Other InfoWe also have studies for Schizophrenia, Depression, Anxiety, ADHD in adults and children, Migraines, Fibromyalgia, and Healthy adults.
NotesWe can assist you with transportation if needed.

YOU TUBE - CRY FOR HELP

Study 1475 :Generalized Anxiety Disorder
New Jersey


Type of StudyCRI Worldwide is conducting a research study of an investigational medication for anxiety sufferers.
Aim of StudyThe purpose of this study is to look at the Efficacy and Safety of the medication compared to a placebo.
Inclusion CriteriaTo qualify you must be between the ages of 18 and 65 and currently taking medication to treat your anxiety.
Exclusion CriteriaParticipating in another research study in the last 30 days.
Any type of seizure disorder.
AreaClementon, New Jersey
DurationUp to 12 Weeks
ReimbursementParticipants who qualify and enroll in the study will receive $30.00 per visit.
Other InfoWe also have studies for Schizophrenia, Depression, Anxiety, ADHD in adults and children, Migraines, Fibromyalgia, and Healthy adults.
NotesWe can assist you with transportation if needed.

YOU TUBE - CRY FOR HELP

Study 1445 :Lubricant Eye Drops Trial
London


Study Added: 05/02/2008
Type of Study Independent research group in Westminster SW1 urgently looking for volunteers to take part in a clinical trial approved by an independent ethics committee.
Aim of Study To evaluate the effect of the repeated usage of two lubricant eye drops approved, CE marked and currently marketed in Europe.
Inclusion Criteria Males and Females
Area Volunteers from the London area only.
Duration One month.
Reimbursement If suitable, all products (eyedrops etc..) and services will be provided free of charge in return for participation. Compensation for time and travel will be available.
Other InfoYOU TUBE ABOVE - I love more than you'll ever know by Will Young
NotesAPPLY BELOW

Study 1401 :Do You Suffer from MIld Acne ?
Leeds - Yorkshire


Download volunteer information
Study Added: 15/08/2007
Type of StudyNON INVASIVE

We are conducting a study to investigate the effects of dietary supplements on skin blemishes and spots.
Inclusion Criteria For this study we are looking for volunteers who have approximately 15-20 spots on the face, to take dietary supplements in capsule form and apply a topical gel every day for 12 weeks. You will be required to visit us at the start of the study and after 6 and 12 weeks, to have your skin assessed. You will also have to provide a urine sample at each visit so that we can see how your body is handling the nutrients in the capsules.

Subjects with mild acne vulgaris of the face with an acne grade of no more than 3.0 (O’Brien, Lewis and Cunliffe).
Subjects of either sex aged between 18 years and above.
Subjects who are willing and able to provide written informed consent.
Subject agreeing not to apply/take any other acne treatment throughout the duration of the study.
Subjects agreeing not to use sun-beds or undergo any UV light treatment and to minimise the amount of exposure to direct sunlight for the duration of the study.
Subject not following any dietary regime including vegetarian and vegan diets.
Subject’s willing to take the capsules, being aware the outer shell is made of gelatine.
Subjects agree not to take any additional food supplementary from those dispense during the study, for the 12 week study period. This includes antioxidants and dietary supplements including oils, vitamins, plant extracts, etc.

Exclusion Criteria Subjects using anti-androgen containing contraceptives.
Subjects who during the past month have received oral or topical steroids, oral or topical antibiotics, or acne treatment of any type, including natural or artificial UV therapy.
Subjects currently taking Warfarin Medication
Subjects with a past medical history of diabetic or psoriatic conditions, cancer of any type, or acute conditions of hepatic, renal; cardiac, pulmonary, digestive, haematological, neurological, thyroidal or psychiatric disease. This also applies to subjects with eczema, allergic rashes, bacterial or fungal infections of the facial skin: or other disease of the facial skin.
Subjects with any known or medically diagnosed food allergy.
Subjects with any known or medically diagnosed drug allergy
Subjects who are taking any concomitant medication that may interfere with study evaluation
A recent history (last 12 months) or strong potential for substance abuse including alcohol.
Subjects who have participated in a clinical trial involving a drug within 30 days of recruitment into the study (or are likely to do so at any time during their participation).
Area Leeds, West Yorkshire
Duration The study lasts for 12 weeks mostly using the treatment at home with only 3 visits to the clinic
Reimbursement To Be Confirmed
Other Info SEE NOTES FOR VOLUNTEERS ON THE INFO NOTES BUTTON ABOVE
Notes EXCLUSIVE TO BIOTRAX PORTAL WEB SITES

Study 1390 :Healthy Male Volunteers
Cambridge
Study Added: 07/06/2007
Type of StudyRecruits throughout the year, healthy volunteers to take part in a range of medical trials. On this occasion we are looking for healthy non smoking males aged between 18-45.
Inclusion Criteria Healthy males aged between 18-45 and Non-smokers onto their panel to take part in a range of phase 1, 2 and experimental medicines trials

BMI 18-30
Non Smokers
No regular medication.
Area East Anglia, UK
Cambridge, Cambs
Huntingdon,Peterborough,Harlow,Ely,Norwich,Ipswich
Duration Various ongoing dates
Reimbursement Amount varies depending on study £200-£2000. Travel expenses also paid.
Other Info Recruits from London, Cambridge, Colchester, Chelmsford, Harlow, Stevenage, Milton Keynes, Brentwood, St Edmonds, Peterborough, Essex, Bedfordshire, Norwich, Ipswich, Northampton, Luton, Hertfordshire, Welwyn Garden City, Huntingdon,Ely and anywhere in East Anglia
Notes APPLY BELOW

APPLY ON THE APPLY BUTTON AND YOU WILL NOT HAVE TO COMPLETE FORMS AGAIN. YOU WILL ALSO BE GIVEN THE OPPORTUNITY TO UPDATE YOUR PROFILE IF YOUR CIRCUMSTANCES HAVE CHANGED I.E , YOU HAVE GIVEN UP SMOKING OR CHANGED ADDRESS or E-MAIL ADDRESS ETC

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Study 1382 :Post Menopausal Females needed UK Wide
Leeds - Yorkshire


Study Added: 22/05/2007
Type of StudyUK Clinical Trials, Medical Trials for Post Menopausal Females. A large variety of upcoming clinical studies in the very near future

ARE YOU FIT AND HEALTHY AND ON NO MEDICATIONS ?

EVERY YEAR, THOUSANDS OF PEOPLE MAKE MEDICAL RESEARCH ADVANCES POSSIBLE.....
Aim of StudyEvery day we are making new progress, in treatments for disease such as daibetes, epilepsy, amgina, arthiritis, Parkinson's, osteoporosis, Alzheimer's disease, asthma, diabetes and psoriasis.

This is only possible with the help of people like you.

Volunteers in testing new medications are ordinary people, from students to retired professionals, firemen to backpackers.
Inclusion Criteria Post Menopausal & Surgically Sterilised Females in good general health.

So If you are fit healthy you may be eligible and we would like to here from you
Area We recruit from Leeds, West Yorkshire, UK and we recruit study participants from all over the UK including North Yorkshire, West Yorkshire, South Yorkshire, East Yorkshire, Sheffield, Derby, Newcastle, Nottingham, York, Bradford, Halifax, Huddersfield, Wakefield, Doncaster , Grimsby, Hull, Harrogate, Scunthorpe, Grimsby, Stoke, Scarborough, Cheshire, Liverpool etc etc
DurationWHAT DOES IT INVOLVE

The majority of these studies involve a residential stay, followed by a number of non-residential visits. The length of the stay and number of visits are dependant on each study.
Reimbursement Up to £100 a day
NotesEvery day people are making a real difference to medical breakthroughs.

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Study 1360 :Healthy Volunteers - Males and Females
Utah
Study Added: 05/05/2007
Type of StudyACR are always looking for healthy volunteers for Clinical Trials , Medical Trials, so register on their datbase below to be notified of any studies you may be eligible for.
Inclusion Criteria Males and Females aged 18 - 85

Must pass instant eligibility test on application.
Area West Jordan, Utah, UT
Duration Varies depending on the study.
Reimbursement Payment for time, travel and inconvenience.
Other InfoRecruits from West Jorden, Salt Lake City, St. George, Ogden, Provo, Moab, Logan, Park City, Orem, Cedar City, Kanab, Springdale, Sandy, Green River, Price, Panguitch, Beaver, Iron, Sevier, Box, Elder, Juab, Summit, Cache, Kane, Tooele, Carbon, Millard, Uintah, Daggett, Morgan, Utah, Davis, Piute, Wasatch, Duchesne, Rich, Washington, Emery, Salt Lake, Wayne, Garfield, San Juan, Weber,
Grand, Sanpete or aywhere in UT.
NotesACR Studies are exclusive to Biotrax Portal web sites.

Study 1329 :Surgically Sterile Females Needed UK Wide
Manchester


Study Added: 12/06/2008
Type of StudyUK Clinical Trials, Medical Trials for Surgically Sterile Females. A large variety of upcoming clinical studies in the very near future

ARE YOU FIT AND HEALTHY AND ON NO MEDICATIONS ?

EVERY YEAR, THOUSANDS OF PEOPLE MAKE MEDICAL RESEARCH ADVANCES POSSIBLE.....
Aim of StudyEvery day we are making new progress, in treatments for disease such as daibetes, epilepsy, amgina, arthiritis, Parkinson's, osteoporosis, Alzheimer's disease, asthma, diabetes and psoriasis.

This is only possible with the help of people like you.

Volunteers in testing new medications are ordinary people, from students to retired professionals, firemen to backpackers.
Inclusion Criteria Surgically Sterilised Females in good general health.

So If you are fit healthy you may be eligible and we would like to here from you

Area We recruit from Leeds, West Yorkshire, UK and we recruit study participants from all over the UK including North Yorkshire, West Yorkshire, South Yorkshire, East Yorkshire, Sheffield, Derby, Newcastle, Nottingham, York, Bradford, Halifax, Huddersfield, Wakefield, Doncaster , Grimsby, Hull, Harrogate, Scunthorpe, Grimsby, Stoke, Scarborough, Cheshire, Liverpool etc etc
Duration
Reimbursement Up to £100 a day
Other InfoWHAT DOES IT INVOLVE

The majority of these studies involve a residential stay, followed by a number of non-residential visits. The length of the stay and number of visits are dependant on each study.
NotesEvery day people are making a real difference to medical breakthroughs.

YOU TUBE ABOVE - UNDER THE BOARD WALK - BETTE MIDLLER

Study 1316 :Healthy Male and Female Military Veterans from Operations OIF/OEF 18 - 45
Connecticut


Download volunteer information  
Study Added: 05/11/2007
Type of StudyThe use of propranolol to block memory reconsolidation in PTSD
Aim of StudyDo you have Upsetting Memories from your Deployment in Iraq or Afghanistan?

If so, Female and Male Veterans from Operations OIF/OEF are invited to participate in this research study. This study will be using one day’s dose of a beta-blocker medication (propranolol) to see if it has an effect on upsetting deployment memories.
Inclusion Criteria Male and Female Military Veterans from Operations OIF/OEF
Ages 18-45
Medically Healthy
Exclusion Criteria Non military personnel- No healthy civilian participants are needed at this time.
Currently taking prescription medication (including birth control pills) that could contraindicate with propranolol.
Current illicit substance use or alcohol consumption (as determined by a urine toxicology and alcohol breath test at each session).
Any current or existing psychotic disorders, bipolar disorder, or alcohol dependence.
Active enrollment into any psychiatric or psychological treatment.
Abnormal EKG (EKG is provided by the study).
Any medical conditions discovered in a full physical contraindicating the use of propranolol (a physical is provided by the study).
Diabetic, Asthmatic, or Pregnant
Area New Haven, Connecticut
Duration 4 sessions, for approximately 3-3 ½ hours per session.
Reimbursement $100 per session for a possible total payment of $400
Other InfoInterested in hearing more? Additional information about the study is provided by selecting “info notes” or informed consent” above (e.g. information about propranolol, about each session, etc…). Please contact us with any questions or concerns.

Results of all study material will remain confidential and kept in a secure location that only that Principal Investigator will have access to.

IF YOU KNOW OF ANY MALE OR FEMALE VETRANS WHY NOT E-MAIL THEM THIS STUDY BELOW - YOU CAN EMAIL UP TO 3 FRIENDS NOW .

VIEW REAL INFORMED CONSENT DOCUMENTS ABOVE

MALE INFORMED CONSENT UNDER - INFO NOTES
FEMALE INFORMED CONSENT UNDER - INFORMED CONSENT


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Notes

Study 1279 :Sensory and Consumer Studies
Surrey


Type of StudyNutritional Studies, Research and Consumer Product Testing, Food & Drink Nutrition.

Consumer vocabulary, describing fruits and vegetables texture.
Attitudes to organic foods.
Healthy ageing: texture perception and eating difficulties in the over 60’s.
Consumer understanding of ambiguous terms such as “natural”, “wholesome” etc.
Various commercial projects for individual food companies (confidential), including tastings on French fries, gravy sauces, cracker biscuits.
Aim of Study Leatherhead Food International is a leading research consultancy for the food and drink industry.

We are always looking for volunteers in the Leatherhead and surrounding area to assist us with our nutrition studies. If you are interested in registering to become a volunteer, please contact us. Once registered your details will be kept on our confidential Volunteer Database, which is accessible by our nutrition research staff only.
Inclusion Criteria MALES AND FEMALES
AGED 18 AND ABOVE
The nutrition studies vary in volunteer exclusion and inclusion criteria and our researchers will decide whether or not you are suitable to participate in a particular study. If approached, you just need to decide whether or not you wish to wish to take part.
Area Area Leatherhead and surrounding areas - Ashtead, Dorking, Epsom, Ewell, Sutton, Cobham or Guildford in Surrey

Participants must not be from outside of these areas and within the 10 mile radius of Leatherhead
Duration Short term studies from hours to days
Reimbursement Volunteers are paid for their time. The amount paid varies depending on the study.
Other Info Studies are undertaken in our Human Nutrition Research Unit at Randalls Road, Leatherhead, Surrey located near Leatherhead railway station. It is a relaxed and friendly environment with TV and computer areas and a small garden. The time you need to stay in the Unit varies by study but is usually no more than a few hours and we do not undertake residential studies.

All of our studies are approved by a Local Regional Ethics Committee.

YOU TUBE ABOVE - JENNIFER PAGE CRUSH
NotesAPPLY BELOW

Study 1170 :CTLS - NON SYSTEMIC PAID BLOOD DONATION
London


Type of StudyTAKE A LUNCH BREAK - DONATE BLOOD - GET PAID
Inclusion Criteria Male or female volunteers aged 18-54 years.
Weight above 52kg.
Ability to provide identification.
In good physical health – no current physical illness / infection.
Fasted for at least four and not for longer than 12 hours before blood collection, unless they are specifically donating for DFP that calls for a 24 hours fast. If volunteers have not complied with fasting requirements, their appointment must be rescheduled.
No recent blood donation, either at CTLS or elsewhere (including as part of a trial).
Provided written consent to donate blood and to undergo an HIV test.
Completed DFP Source Document acceptable to screening staff and confirming absence of conditions that may make donation hazardous.
Vital signs within reference range, or acceptable to screening staff.
Negative breath alcohol and carbon monoxide tests.
Negative urine drugs-of-abuse tests (opiates, amphetamines, cocaine metabolites, cannabinoids, benzodiazepines, barbiturates).
Negative pregnancy test if female.
Volunteers must be taking no regular medication (including over the counter medication). This excludes all women using hormonal contraceptives.
Volunteers must have taken no medication (including over the counter medication) within the 14 days prior to donation.
Area Volunteers from London only please .
Duration 1 hour to 1.5 hours at the most
Reimbursement Up to £60 depending on how much blood you donate.
Donations may only be 100mls or up to a pint depending on whether you are prepared to fast for 24hrs prior to donation.

Discuss your options with CTLS highly qualified staff
Free Gift
Other Info VOLUNTEERS IN DRUG TRIALS OR CONSIDERING DRUG TRIALS SHOULD NOT APPLY
VOLUNTEERS IN NON INVASIVE RESEARCH STUDIES WILL BE ACCEPTABLE
NotesTHE RECRUITMENT OF THIS RESEARCH IS EXCLUSIVE TO BIOTRAX

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Study 864 :Stress and Health Studies.
Ohio