Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
4,882
archived clinical trials in
Obesity Weight Loss

Women's Health Project for Women Wanting to Lose Weight
Intervention Study in Women Wanting to Lose Weight (Women's Health Project)
Status: Enrolling
Updated:  4/17/2013
Texas Tech Health Sciences Center - Physicians Pavillion, Internal Medicine Clinic
mi
from
Lubbock, TX
Women's Health Project for Women Wanting to Lose Weight
Intervention Study in Women Wanting to Lose Weight (Women's Health Project)
Status: Enrolling
Updated: 4/17/2013
Texas Tech Health Sciences Center - Physicians Pavillion, Internal Medicine Clinic
mi
from
Lubbock, TX
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Access to Nutritional Services and the Effect on Maternal Weight Gain
Ease of Access to Nutritional Services and the Effect on Maternal Weight in an Obese Urban Population
Status: Enrolling
Updated:  4/18/2013
Abington Memorial Hospital
mi
from
Abington, PA
Access to Nutritional Services and the Effect on Maternal Weight Gain
Ease of Access to Nutritional Services and the Effect on Maternal Weight in an Obese Urban Population
Status: Enrolling
Updated: 4/18/2013
Abington Memorial Hospital
mi
from
Abington, PA
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Access to Nutritional Services and the Effect on Maternal Weight Gain
Ease of Access to Nutritional Services and the Effect on Maternal Weight in an Obese Urban Population
Status: Enrolling
Updated:  4/18/2013
Abington Memorial Hospital
mi
from
Abington, PA
Access to Nutritional Services and the Effect on Maternal Weight Gain
Ease of Access to Nutritional Services and the Effect on Maternal Weight in an Obese Urban Population
Status: Enrolling
Updated: 4/18/2013
Abington Memorial Hospital
mi
from
Abington, PA
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Exercise in Breast Cancer Survivors
Exercise in Breast Cancer Survivors: Analysis of Angiogenic Profile
Status: Enrolling
Updated:  4/22/2013
University of Mississippi Health Care
mi
from
Jackson, MS
Exercise in Breast Cancer Survivors
Exercise in Breast Cancer Survivors: Analysis of Angiogenic Profile
Status: Enrolling
Updated: 4/22/2013
University of Mississippi Health Care
mi
from
Jackson, MS
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The Wildcat Wellness Coaching Trial
The Wildcat Wellness Coaching Trial: Home-based Obesity Prevention and Health Promotion in Children and Adolescents
Status: Enrolling
Updated:  4/30/2013
Physical Activity & Nutrition Clinical Research Consortium
mi
from
Manhattan, KA
The Wildcat Wellness Coaching Trial
The Wildcat Wellness Coaching Trial: Home-based Obesity Prevention and Health Promotion in Children and Adolescents
Status: Enrolling
Updated: 4/30/2013
Physical Activity & Nutrition Clinical Research Consortium
mi
from
Manhattan, KA
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Multiple Dose Safety Tolerability, Pharmacokinetics And Midazolam Interaction In Healthy Overweight And Obese Subjects
A Phase 1 Placebo-Controlled Study To Assess Safety, Tolerability, Pharmacokinetics And Effect On Midazolam Pharmacokinetics Of Multiple Oral Doses Of PF-05175157 Administered In A Tablet Formulation In Otherwise Healthy Overweight And Obese Subjects
Status: Enrolling
Updated:  5/6/2013
Pfizer Investigational Site
mi
from
Los Angeles, CA
Multiple Dose Safety Tolerability, Pharmacokinetics And Midazolam Interaction In Healthy Overweight And Obese Subjects
A Phase 1 Placebo-Controlled Study To Assess Safety, Tolerability, Pharmacokinetics And Effect On Midazolam Pharmacokinetics Of Multiple Oral Doses Of PF-05175157 Administered In A Tablet Formulation In Otherwise Healthy Overweight And Obese Subjects
Status: Enrolling
Updated: 5/6/2013
Pfizer Investigational Site
mi
from
Los Angeles, CA
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The KP Personal Shopper: A Pilot to Improve the Impact of Dietary Advice
Status: Enrolling
Updated:  5/6/2013
Kaiser Permanente Center for Health Research, Southeast
mi
from
Atlanta, GA
The KP Personal Shopper: A Pilot to Improve the Impact of Dietary Advice
Status: Enrolling
Updated: 5/6/2013
Kaiser Permanente Center for Health Research, Southeast
mi
from
Atlanta, GA
Click here to add this to my saved trials
Safety and Efficacy of Lean Body Weight-based IV Heparin Dosing in Obese/Morbidly Obese Patients
Assessing Safety and Efficacy of Lean Body Weight-based Intravenous Heparin Dosing in Obese/Morbidly Obese Patients. A Pilot Study
Status: Enrolling
Updated:  5/13/2013
Nazareth Hospital - Mercy Health System
mi
from
Philadelphia, PA
Safety and Efficacy of Lean Body Weight-based IV Heparin Dosing in Obese/Morbidly Obese Patients
Assessing Safety and Efficacy of Lean Body Weight-based Intravenous Heparin Dosing in Obese/Morbidly Obese Patients. A Pilot Study
Status: Enrolling
Updated: 5/13/2013
Nazareth Hospital - Mercy Health System
mi
from
Philadelphia, PA
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Feasibility of Use of BariCare App in Pre-bariatric Surgery.
Feasibility and Efficacy of Engagement Modules for Pre-Bariatric Surgery Patients.
Status: Enrolling
Updated:  5/17/2013
Mayo Clinic Rochester
mi
from
Rochester, MN
Feasibility of Use of BariCare App in Pre-bariatric Surgery.
Feasibility and Efficacy of Engagement Modules for Pre-Bariatric Surgery Patients.
Status: Enrolling
Updated: 5/17/2013
Mayo Clinic Rochester
mi
from
Rochester, MN
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Nutrigenomics: Personalizing Weight Loss for Obese Veterans
Nutrigenomics: Personalizing Weight Loss for Obese Veterans
Status: Enrolling
Updated:  5/17/2013
VA San Diego Healthcare System
mi
from
San Diego, CA
Nutrigenomics: Personalizing Weight Loss for Obese Veterans
Nutrigenomics: Personalizing Weight Loss for Obese Veterans
Status: Enrolling
Updated: 5/17/2013
VA San Diego Healthcare System
mi
from
San Diego, CA
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Comparison of Tissue Retractors During Cesarean Delivery in Obese Women
Randomized Controlled Trial of the Efficacy of the Mobius ™ Retractor in Performing Cesarean Sections in Patients With BMI ≥35kg/m2
Status: Enrolling
Updated:  5/20/2013
Thomas Jefferson University
mi
from
Philadelphia, PA
Comparison of Tissue Retractors During Cesarean Delivery in Obese Women
Randomized Controlled Trial of the Efficacy of the Mobius ™ Retractor in Performing Cesarean Sections in Patients With BMI ≥35kg/m2
Status: Enrolling
Updated: 5/20/2013
Thomas Jefferson University
mi
from
Philadelphia, PA
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Health Benefits of Chronic vs. Acute Exercise in Overweight Adults
Status: Enrolling
Updated:  6/17/2013
Substrate Metabolism Laboratory
mi
from
Ann Arbor, MI
Health Benefits of Chronic vs. Acute Exercise in Overweight Adults
Status: Enrolling
Updated: 6/17/2013
Substrate Metabolism Laboratory
mi
from
Ann Arbor, MI
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Children's Healthy Living Program
Children's Healthy Living Program for Remote Underserved Minority Populations in the Pacific Region
Status: Enrolling
Updated:  6/18/2013
Univ of Hawaii
mi
from
Honolulu, HI
Children's Healthy Living Program
Children's Healthy Living Program for Remote Underserved Minority Populations in the Pacific Region
Status: Enrolling
Updated: 6/18/2013
Univ of Hawaii
mi
from
Honolulu, HI
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Studying the Effects of Phentermine on Eating Behavior
The Quantification of Ingestive Behavior
Status: Enrolling
Updated:  6/24/2013
The New York State Psychiatric Institute at Columbia University Medical Center
mi
from
New York, NY
Studying the Effects of Phentermine on Eating Behavior
The Quantification of Ingestive Behavior
Status: Enrolling
Updated: 6/24/2013
The New York State Psychiatric Institute at Columbia University Medical Center
mi
from
New York, NY
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Effects of TNF-alpha Antagonism (Etanercept) in Patients With the Metabolic Syndrome and Psoriasis
Effects of TNF-alpha Antagonism (Etanercept) in Patients With the Metabolic Syndrome and Psoriasis
Status: Enrolling
Updated:  6/25/2013
Massachusetts General Hospital
mi
from
Boston, MA
Effects of TNF-alpha Antagonism (Etanercept) in Patients With the Metabolic Syndrome and Psoriasis
Effects of TNF-alpha Antagonism (Etanercept) in Patients With the Metabolic Syndrome and Psoriasis
Status: Enrolling
Updated: 6/25/2013
Massachusetts General Hospital
mi
from
Boston, MA
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Comparison of Body Composition & Weight Change in Users of Progestin-only Contraception During the First Year of Use
Comparison of Body Composition & Weight Change in Users of Progestin-only Contraception During the First Year of Use
Status: Enrolling
Updated:  6/25/2013
Washington University School of Medicine
mi
from
Saint Louis, MO
Comparison of Body Composition & Weight Change in Users of Progestin-only Contraception During the First Year of Use
Comparison of Body Composition & Weight Change in Users of Progestin-only Contraception During the First Year of Use
Status: Enrolling
Updated: 6/25/2013
Washington University School of Medicine
mi
from
Saint Louis, MO
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Loss of Grip Strength, BMI, and Adjuvant Endocrine Therapy Breast Cancer
A Prospective Assessment of Loss of Grip Strength by Baseline BMI in Breast Cancer Patients Receiving Adjuvant Third-generation Aromatase Inhibitors and Tamoxifen
Status: Enrolling
Updated:  7/5/2013
University of Michigan Comprehensive Cancer Center
mi
from
Ann Arbor, MI
Loss of Grip Strength, BMI, and Adjuvant Endocrine Therapy Breast Cancer
A Prospective Assessment of Loss of Grip Strength by Baseline BMI in Breast Cancer Patients Receiving Adjuvant Third-generation Aromatase Inhibitors and Tamoxifen
Status: Enrolling
Updated: 7/5/2013
University of Michigan Comprehensive Cancer Center
mi
from
Ann Arbor, MI
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Niños Sanos, Familia Sana - A Multi-Intervention Program to Prevent Childhood Obesity in Mexican-Heritage Children in Rural California
Niños Sanos, Familia Sana (Healthy Children/Healthy Family): A Multi-Intervention Program to Prevent Childhood Obesity in Mexican-Heritage Children in Rural California
Status: Enrolling
Updated:  7/15/2013
UC Davis
mi
from
Davis, CA
Niños Sanos, Familia Sana - A Multi-Intervention Program to Prevent Childhood Obesity in Mexican-Heritage Children in Rural California
Niños Sanos, Familia Sana (Healthy Children/Healthy Family): A Multi-Intervention Program to Prevent Childhood Obesity in Mexican-Heritage Children in Rural California
Status: Enrolling
Updated: 7/15/2013
UC Davis
mi
from
Davis, CA
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Feeding Trial in the Obese Critical Care Population
Enteral Formula Tolerance in the Obese Critical Care Population
Status: Enrolling
Updated:  7/16/2013
University of Kentucky
mi
from
Lexington, KY
Feeding Trial in the Obese Critical Care Population
Enteral Formula Tolerance in the Obese Critical Care Population
Status: Enrolling
Updated: 7/16/2013
University of Kentucky
mi
from
Lexington, KY
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Feeding Trial in the Obese Critical Care Population
Enteral Formula Tolerance in the Obese Critical Care Population
Status: Enrolling
Updated:  7/16/2013
University of Louisville
mi
from
Louisville, KY
Feeding Trial in the Obese Critical Care Population
Enteral Formula Tolerance in the Obese Critical Care Population
Status: Enrolling
Updated: 7/16/2013
University of Louisville
mi
from
Louisville, KY
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Teen CHAT: Improving Physician Communication With Adolescents About Healthy Weight
Teen CHAT: Improving Physician Communication With Adolescents About Healthy Weight
Status: Enrolling
Updated:  7/22/2013
Duke University Medical Center - Cancer Prevention, Detection and Control
mi
from
Durham, NC
Teen CHAT: Improving Physician Communication With Adolescents About Healthy Weight
Teen CHAT: Improving Physician Communication With Adolescents About Healthy Weight
Status: Enrolling
Updated: 7/22/2013
Duke University Medical Center - Cancer Prevention, Detection and Control
mi
from
Durham, NC
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Effects of Monosodium Glutamate on Energy Balance and Eating Behavior
Effects of Ingesting Monosodium Glutamate (MSG) on Energy Balance and Eating Behavior Following Moderate Energy Restriction and Weight Loss in Overweight Women
Status: Enrolling
Updated:  7/22/2013
Western Human Nutrition Center, University of California Davis
mi
from
Davis, CA
Effects of Monosodium Glutamate on Energy Balance and Eating Behavior
Effects of Ingesting Monosodium Glutamate (MSG) on Energy Balance and Eating Behavior Following Moderate Energy Restriction and Weight Loss in Overweight Women
Status: Enrolling
Updated: 7/22/2013
Western Human Nutrition Center, University of California Davis
mi
from
Davis, CA
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An Efficacy, Safety, and Pharmacokinetics Study of Beloranib in Obese Subjects With Prader-Willi Syndrome
Randomized, Double-Blind, Placebo Controlled, Parallel Dose Ranging Phase 2a Trial of ZGN-440 (Subcutaneous Beloranib in Suspension), A Novel Methionine Aminopeptidase 2 Inhibitor, in Over-weight and Obese Subjects With Prader-Willi Syndrome to Evaluate Weight Reduction, Food-related Behavior, Safety, and Pharmacokinetics Over 4 Weeks Followed by Optional 4-Week Open-Label Extension
Status: Enrolling
Updated:  7/22/2013
University of Florida
mi
from
Gainesville, FL
An Efficacy, Safety, and Pharmacokinetics Study of Beloranib in Obese Subjects With Prader-Willi Syndrome
Randomized, Double-Blind, Placebo Controlled, Parallel Dose Ranging Phase 2a Trial of ZGN-440 (Subcutaneous Beloranib in Suspension), A Novel Methionine Aminopeptidase 2 Inhibitor, in Over-weight and Obese Subjects With Prader-Willi Syndrome to Evaluate Weight Reduction, Food-related Behavior, Safety, and Pharmacokinetics Over 4 Weeks Followed by Optional 4-Week Open-Label Extension
Status: Enrolling
Updated: 7/22/2013
University of Florida
mi
from
Gainesville, FL
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Effects of Intentional Weight Loss Interventions in Chronic Kidney Disease
Effects of Intentional Weight Loss Interventions in Chronic Kidney Disease
Status: Enrolling
Updated:  7/29/2013
Cleveland Clinic
mi
from
Cleveland, OH
Effects of Intentional Weight Loss Interventions in Chronic Kidney Disease
Effects of Intentional Weight Loss Interventions in Chronic Kidney Disease
Status: Enrolling
Updated: 7/29/2013
Cleveland Clinic
mi
from
Cleveland, OH
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The Effects of Mindsets on the Brain's Response to Food Cues
The Effects of Mindsets on the Brain's Response to Food Cues
Status: Enrolling
Updated:  7/30/2013
Weight Control and Diabetes Research Center
mi
from
Providence, RI
The Effects of Mindsets on the Brain's Response to Food Cues
The Effects of Mindsets on the Brain's Response to Food Cues
Status: Enrolling
Updated: 7/30/2013
Weight Control and Diabetes Research Center
mi
from
Providence, RI
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Maternal, Adiposity, Metabolism, and Stress Study
Maternal, Adiposity, Metabolism, and Stress Study (MAMAS)
Status: Enrolling
Updated:  8/1/2013
University of California - San Francisco
mi
from
San Francisco, CA
Maternal, Adiposity, Metabolism, and Stress Study
Maternal, Adiposity, Metabolism, and Stress Study (MAMAS)
Status: Enrolling
Updated: 8/1/2013
University of California - San Francisco
mi
from
San Francisco, CA
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Postprandial Response to Almond Consumption in Overweight Hispanic Pregnant Women
Postprandial Response to Almond Consumption in Overweight Hispanic Pregnant Women
Status: Enrolling
Updated:  8/9/2013
Children's Hospital Oakland Research Institute
mi
from
Oakland, CA
Postprandial Response to Almond Consumption in Overweight Hispanic Pregnant Women
Postprandial Response to Almond Consumption in Overweight Hispanic Pregnant Women
Status: Enrolling
Updated: 8/9/2013
Children's Hospital Oakland Research Institute
mi
from
Oakland, CA
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miRNA in Fetal Overgrowth
Placental miRNA (microRNA) Profile in Fetal Overgrowth Related to Maternal Obesity Study
Status: Enrolling
Updated:  8/29/2013
Hospital of the University of Pennsylvania
mi
from
Philadelphia, PA
miRNA in Fetal Overgrowth
Placental miRNA (microRNA) Profile in Fetal Overgrowth Related to Maternal Obesity Study
Status: Enrolling
Updated: 8/29/2013
Hospital of the University of Pennsylvania
mi
from
Philadelphia, PA
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Stress Reduction for Overweight or Obese Women Either With Polycystic Ovary Syndrome (PCOS) or Without PCOS (Non-PCOS)
Stress Reduction for PCOS and Non-PCOS Women
Status: Enrolling
Updated:  9/7/2013
Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
Stress Reduction for Overweight or Obese Women Either With Polycystic Ovary Syndrome (PCOS) or Without PCOS (Non-PCOS)
Stress Reduction for PCOS and Non-PCOS Women
Status: Enrolling
Updated: 9/7/2013
Penn State Milton S. Hershey Medical Center
mi
from
Hershey, PA
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Reducing Weight Gain and Improving Metabolic Function in Children Being Treated With Antipsychotics
Improving Metabolic Parameters of Antipsychotic Child Treatment
Status: Enrolling
Updated:  9/21/2013
Johns Hopkins Hosp
mi
from
Baltimore, MD
Reducing Weight Gain and Improving Metabolic Function in Children Being Treated With Antipsychotics
Improving Metabolic Parameters of Antipsychotic Child Treatment
Status: Enrolling
Updated: 9/21/2013
Johns Hopkins Hosp
mi
from
Baltimore, MD
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Reducing Weight Gain and Improving Metabolic Function in Children Being Treated With Antipsychotics
Improving Metabolic Parameters of Antipsychotic Child Treatment
Status: Enrolling
Updated:  9/21/2013
University of Maryland
mi
from
Baltimore, MD
Reducing Weight Gain and Improving Metabolic Function in Children Being Treated With Antipsychotics
Improving Metabolic Parameters of Antipsychotic Child Treatment
Status: Enrolling
Updated: 9/21/2013
University of Maryland
mi
from
Baltimore, MD
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Reducing Weight Gain and Improving Metabolic Function in Children Being Treated With Antipsychotics
Improving Metabolic Parameters of Antipsychotic Child Treatment
Status: Enrolling
Updated:  9/21/2013
The Zucker Hillside Hospital
mi
from
Glen Oaks, NY
Reducing Weight Gain and Improving Metabolic Function in Children Being Treated With Antipsychotics
Improving Metabolic Parameters of Antipsychotic Child Treatment
Status: Enrolling
Updated: 9/21/2013
The Zucker Hillside Hospital
mi
from
Glen Oaks, NY
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Reducing Weight Gain and Improving Metabolic Function in Children Being Treated With Antipsychotics
Improving Metabolic Parameters of Antipsychotic Child Treatment
Status: Enrolling
Updated:  9/21/2013
University of North Carolina, Division of Child and Adolescent Psychiatry
mi
from
Chapel Hill, NC
Reducing Weight Gain and Improving Metabolic Function in Children Being Treated With Antipsychotics
Improving Metabolic Parameters of Antipsychotic Child Treatment
Status: Enrolling
Updated: 9/21/2013
University of North Carolina, Division of Child and Adolescent Psychiatry
mi
from
Chapel Hill, NC
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Weight Loss Study for Patients With Obesity Due to Craniopharyngioma or Other Brain Tumor
Effects of Exenatide on Body Weight in Patients With Hypothalamic Obesity
Status: Enrolling
Updated:  10/23/2013
Vanderbilt University
mi
from
Nashville, TN
Weight Loss Study for Patients With Obesity Due to Craniopharyngioma or Other Brain Tumor
Effects of Exenatide on Body Weight in Patients With Hypothalamic Obesity
Status: Enrolling
Updated: 10/23/2013
Vanderbilt University
mi
from
Nashville, TN
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Endoscopic Suturing for Primary Obesity Treatment
Primary Obesity Multicenter Incisionless Suturing Evaluation: The PROMISE Trial
Status: Enrolling
Updated:  10/23/2013
Jackson Health System
mi
from
Miami, FL
Endoscopic Suturing for Primary Obesity Treatment
Primary Obesity Multicenter Incisionless Suturing Evaluation: The PROMISE Trial
Status: Enrolling
Updated: 10/23/2013
Jackson Health System
mi
from
Miami, FL
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Endoscopic Suturing for Primary Obesity Treatment
Primary Obesity Multicenter Incisionless Suturing Evaluation: The PROMISE Trial
Status: Enrolling
Updated:  10/23/2013
Brigham and Women's Hosp
mi
from
Boston, MA
Endoscopic Suturing for Primary Obesity Treatment
Primary Obesity Multicenter Incisionless Suturing Evaluation: The PROMISE Trial
Status: Enrolling
Updated: 10/23/2013
Brigham and Women's Hosp
mi
from
Boston, MA
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Endoscopic Suturing for Primary Obesity Treatment
Primary Obesity Multicenter Incisionless Suturing Evaluation: The PROMISE Trial
Status: Enrolling
Updated:  10/23/2013
St. Joseph's Regional Medical Center at New Jersey
mi
from
Paterson, NJ
Endoscopic Suturing for Primary Obesity Treatment
Primary Obesity Multicenter Incisionless Suturing Evaluation: The PROMISE Trial
Status: Enrolling
Updated: 10/23/2013
St. Joseph's Regional Medical Center at New Jersey
mi
from
Paterson, NJ
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Endoscopic Suturing for Primary Obesity Treatment
Primary Obesity Multicenter Incisionless Suturing Evaluation: The PROMISE Trial
Status: Enrolling
Updated:  10/23/2013
University of Texas at Houston
mi
from
Bellaire, TX
Endoscopic Suturing for Primary Obesity Treatment
Primary Obesity Multicenter Incisionless Suturing Evaluation: The PROMISE Trial
Status: Enrolling
Updated: 10/23/2013
University of Texas at Houston
mi
from
Bellaire, TX
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Healthy Growth Abbreviated Pilot Study
Abbreviated Pilot Trial of a Peer-Based Social Media Intervention to Promote Healthy Growth During Infancy
Status: Enrolling
Updated:  10/30/2013
Children's Hospital of Philadelphia
mi
from
Philadelphia, PA
Healthy Growth Abbreviated Pilot Study
Abbreviated Pilot Trial of a Peer-Based Social Media Intervention to Promote Healthy Growth During Infancy
Status: Enrolling
Updated: 10/30/2013
Children's Hospital of Philadelphia
mi
from
Philadelphia, PA
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Effect of Vitamin D Supplementation on Endothelial Function in Obese Adolescents
Effect of Vitamin D Supplementation on Endothelial Function in Obese Adolescents
Status: Enrolling
Updated:  11/11/2013
Mayo Clinic Rochester
mi
from
Rochester, MN
Effect of Vitamin D Supplementation on Endothelial Function in Obese Adolescents
Effect of Vitamin D Supplementation on Endothelial Function in Obese Adolescents
Status: Enrolling
Updated: 11/11/2013
Mayo Clinic Rochester
mi
from
Rochester, MN
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Characterization of Dyslipidemia in Adolescent Obesity
Characterization of Dyslipidemia in Adolescent Obesity
Status: Enrolling
Updated:  11/13/2013
The Center For Nutrition and Preventive Medicine
mi
from
Charlotte, NC
Characterization of Dyslipidemia in Adolescent Obesity
Characterization of Dyslipidemia in Adolescent Obesity
Status: Enrolling
Updated: 11/13/2013
The Center For Nutrition and Preventive Medicine
mi
from
Charlotte, NC
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Portion Size Strategies for Management of Body Weight
Status: Enrolling
Updated:  11/15/2013
Penn State University Laboratory for the Study of Human Ingestive Behavior
mi
from
University Park, PA
Portion Size Strategies for Management of Body Weight
Status: Enrolling
Updated: 11/15/2013
Penn State University Laboratory for the Study of Human Ingestive Behavior
mi
from
University Park, PA
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A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated:  11/18/2013
University of Alabama at Birmingham
mi
from
Birmingham, AL
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated: 11/18/2013
University of Alabama at Birmingham
mi
from
Birmingham, AL
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A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated:  11/18/2013
Radiant Research - Arizona
mi
from
Chandler, AZ
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated: 11/18/2013
Radiant Research - Arizona
mi
from
Chandler, AZ
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A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated:  11/18/2013
Scripps Clinical Research Center
mi
from
La Jolla, CA
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated: 11/18/2013
Scripps Clinical Research Center
mi
from
La Jolla, CA
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A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated:  11/18/2013
Translational Research Institute for Metabolism and Diabetes
mi
from
Orlando, FL
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated: 11/18/2013
Translational Research Institute for Metabolism and Diabetes
mi
from
Orlando, FL
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A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated:  11/18/2013
Pennington Biomedical Research Center
mi
from
Baton Rouge, LA
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated: 11/18/2013
Pennington Biomedical Research Center
mi
from
Baton Rouge, LA
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A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated:  11/18/2013
Boston Med Center
mi
from
Boston, MA
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated: 11/18/2013
Boston Med Center
mi
from
Boston, MA
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A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated:  11/18/2013
Weill Cornell College
mi
from
New York, NY
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated: 11/18/2013
Weill Cornell College
mi
from
New York, NY
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A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated:  11/18/2013
Duke University
mi
from
Durham, NC
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
A Multicenter Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate- Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
Status: Enrolling
Updated: 11/18/2013
Duke University
mi
from
Durham, NC
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