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Patient Medical Trials, Drug Trials, Clinical Trials, Medical Research, Clinical Research for People with Medical Conditions in

105 studies recruit in and from this area



Study 1613 :Do you have Type 2 Diabetes? - Want to Make a Difference? - Why not Help Medical Research ?
London


Study Added: 30/05/2008
Type of StudyClinical Trials Medical Trials 4 Sufferers of Type 2 Diabetes
Inclusion Criteria Males and Females needed aged 30-65 years
Area To take part in studies conducted at our
clinical research unit based in Slough, Berkshire
Reimbursement You will be paid for the time you spend
with us
Other InfoYOU TUBE ABOVE - Micheal Buble - SWAY
NotesCall: 0800 783 0976 to register
http://www.wanttomakeadifference.com

or Apply Below

Study 1598 : Studies for dry eye sufferers
London


Study Added: 23/05/2008
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 1564 :Type 2 Diabetes - Males & Females 18-60 yrs - Up to $1,950
Texas


 
Study Added: 23/08/2008
Type of StudyHealthcare Discoveries is conducting a research study of an investigational product in male/female volunteers, ages 18-60, with Type II Diabetes..


You may be compensated up to $1,950.00 for time and travel.

Call our recruitment line for more details.

For more information on this study contact our recruitment hotline at 210-CALLHCD (210-225- 5423)

Aim of StudyThis study may help determine the safety and tolerability of the study drig which is being developed for the trestment of Type 2 Diabetes Melitus.. The study drug will be given orally.

Vital signs, ECGs, physical examinations and blood and urine samples will be obtained and performed during this study.

Inclusion Criteria Male/female volunteers, ages 18-60, with Type II Diabetes..
Area San Antonio,Texas, Tx
Duration You will need to complete:

1 screening visit
1 out patient visit
8 overnight visits
1 Follow up visit
Reimbursement You may be compensated up to $1,950.00 for time and travel.

Other InfoCall our recruitment line for more details.

For more information on this study contact our recruitment hotline at 210-CALLHCD (210-225- 5423)

YOU TUBE ABOVE - YOU AND I

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


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.
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 1459 :Bipolar I Depression
New Jersey


Study Added: 28/12/2007
Type of StudyWe are looking for patient volunteers who have Major Depression with Bipolar I disorder that is not responding to current treatment.
Aim of StudyThe purpose of this study is to look at the safety, effectiveness and tolerability of the medication.
Inclusion CriteriaPatients who are between the ages of 18 to 55 years old and are currently taking Depakote, Lithium or Zyprexa (Olanzapine).
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 1373 :The use of propranolol to block memory reconsolidation in PTSD
Connecticut


Download volunteer information  
Study Added: 05/11/2007
Aim of StudyTo see if one day's dose of a beta blocker medication has an effect on upsetting combat memories.
Inclusion CriteriaMale veterans from OIF/OEF
Age 18-45
Exclusion CriteriaCurrent illicit substance use or alcohol consumption (as determined by a urine toxicology and alcohol breath test).
Any currently existing psychotic disorder, bipolar disorder, or alcohol dependence.
Any current prescription medication usage contraindicated with propranolol.
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 (physical is provided by the study).
AreaNew Haven, Connecticut
DurationFour sessions, approximately 4 hours each.
Reimbursement$100 per session for a possible total payment of $400

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


YOU TUBE ABOVE - Tony Bennett and Stevie Wonder - For Once in my life live

Notes

Study 1293 :Research for PTSD and Alcohol Dependence
Connecticut


 
Study Added: 18/11/2008
Type of StudyClinical Research Treatment Study for Veterans
Aim of StudyHave you had a traumatic experience? Do you experience symptoms of Post Traumatic Stress Disorder (flashbacks, nightmares, irritability, sleep problems)? Do you drink regularly? We are testing the effects of medication called Prazosin on alcohol use and symptoms of PTSD.
Inclusion Criteria Men and women who are medically healthy, have symptoms of PTSD, and are currently drinking regularly, are invited to participate in this study.
Exclusion Criteria Any current or existing psychotic disorders (schizophrenia, schizoaffective disorder) and bipolar disorder
Area New Haven, CT
Duration 13 weeks of research treatment sessions and one 3 month follow-up session
Reimbursement Possible total payment of up to $366
Other Info Participation is confidential. To learn more about this study see “informed consent” above, call us via the phone number provided in “contact,” or apply below.
NotesYOU TUBE ABOVE - Close Every Door... Andrew Lloyd Webber

Send to a friend with symptoms

Study 1279 :Sensory and Consumer Studies
Surrey


Study Added: 30/12/2006
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 1264 :Research for Depression and Alcohol Dependence
Connecticut


 
Study Added: 18/11/2008
Type of StudyClinical Research Treatment Study
Aim of StudyDo you feel sad or depressed? Are you tired most of the time? Have you lost interest in things you usually enjoy? Do you currently drink and want to stop? We are testing the effect of a medication called mecamylamine and brief counseling in reducing depressive symptoms and alcohol use.
Inclusion Criteria Men and women who are medically healthy, have symptoms of depression, and are currently drinking regularly, are invited to participate in this study.
Exclusion Criteria Any current or existing psychotic disorders (schizophrenia, schizoaffective disorder) and bipolar disorder
Area New Haven, CT
Duration 13 weeks of research treatment sessions and one 3 month follow-up session
Reimbursement Possible total payment of up to $230
Other Info Participation is confidential. To learn more about this study see “informed consent” above, call us via the phone number provided in “contact,” or apply below.
NotesSEE YOU TUBE ABOVE AND EMAIL TO A FRIEND WITH SYMPTOMS

Cats Musical - Memory

Study 1260 :Major Depressive Disorder
New Jersey


Study Added: 12/01/2008
Type of StudyOur office is currently conducting a research study that involves the use of a drug that it not yet approved by the FDA for patients who suffer with Major Depressive Disorder.
Aim of StudyThe purpose of this study is to look at the efficacy, safety, and tolerability of the medication as well as the response to the medication.
Inclusion CriteriaPatients who are between the ages of 18-55 that are non smokers. BMI must be between 16 and 40.
Exclusion CriteriaParticipating in another research study in the last 30 days.
Any type of seizure disorder.
You can not have Hepatitis B, Hepatitis C, or HIV.
AreaClementon New Jersey
DurationUp to 11 weeks
ReimbursementStudy-related physical exams, laboratory tests, psychiatric evaluations, and study medication or placebo will be provided to you at no cost. There will also be reimbursement for time and travel.
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 1191 :Do you currently drink? Would you like help to stop drinking?
Connecticut


 
Study Added: 18/11/2008
Type of StudyClinical Research Treatment Study
Aim of StudyDo you currently drink and want to stop? We are testing the effect of a medication called mecamylamine and brief counseling in reducing alcohol use.
Inclusion Criteria Men and women who are medically healthy and are currently drinking regularly are invited to participate in this study.
Exclusion Criteria Any current or existing psychotic disorders (schizophrenia, schizoaffective disorder) and bipolar disorder
Area New Haven, CT
Duration 13 weeks of research treatment sessions and one 3 month follow-up session
Reimbursement Possible total payment of up to $230
Other Info Participation is confidential. To learn more about this study see “informed consent” above, call us via the phone number provided in “contact.”
NotesYOU TUBE ABOVE - Dina Carroll - The Perfect Year - Send to friend with symptoms

Study 485 :Food & Drink Nutrition Studies 4 Males/Females Aged 18 & Above
Surrey


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


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 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 - IN PRIVATE - DUSTY SPRINGFIELD
NotesAPPLY BELOW

Study 435 :CEREAL SNACK WEIGHT MANAGEMENT STUDY - Males/Femlaes Aged 18 - 65 Yrs
Surrey