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NCT00710814 · ClinicalTrials.gov registry record · Phase 1

Trial of Leptin Administration After Roux-en-Y Gastric Bypass

A Phase 1 study of Overweight, sponsored by Columbia University.

Completed
Registry status
Phase 1
Development phase
31
Enrollment target
1
Study location

NCT00710814 is a Phase 1 study of Overweight that has completed, run by Columbia University. The registered enrollment target is 31 participants, below the 1,323-participant average among 197 other Overweight trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00710814, a Phase 1 study of Overweight, has completed, sponsored by Columbia University.

COMPLETED
Registry status
Phase 1
Development phase
31 participants
Enrollment target
1
Study location

Study Summary

This is a pilot and feasibility study to examine a novel intervention using leptin in weight-reduced individuals who have undergone bariatric surgery but still remain obese. Leptin, a peptide hormone secreted from adipose tissue, is a regulator of food intake and energy expenditure. Administration of leptin resulted in profound weight reduction in the few reported cases of obese individuals with genetic leptin deficiency. However, most obese people have increased leptin levels. Such individuals are said to be in a "leptin-resistant" state, whereby administration of physiological concentrations of leptin are ineffective at producing significant weight reduction. Roux-en-Y gastric bypass surgery (RYGBP) is more effective than diet alone in producing long-term reduction of body weight. Yet even after surgery there is a plateau in weight loss though the individual may still be obese and have or be at risk for obesity related morbidities. The investigators have shown that plasma leptin levels are significantly lower in women after RYGBP compared with BMI-matched controls. This state of relative hypoleptinemia or leptin insufficiency suggests that post-RYGBP individuals may be in a "leptin-sensitive" state and, thus, would undergo further weight loss when administered doses of leptin that would not normally result in significant weight reduction. This study will examine the effects of leptin administered by self-injection twice per day on body weight and endocrine function. All individuals will received leptin and placebo and different times during the 34 week study period.

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG Leptin

Study Locations (1)

New York

  • Columbia University Medical Center - New York

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2008-04
Est. Completion 2014-07
Phase Phase 1

Sponsor

Columbia University

958 total trials

What the Registry Record Tells You About NCT00710814

The ClinicalTrials.gov registry entry for NCT00710814 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,323-participant average among 197 other Overweight trials with a reported enrollment target (98% lower). The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Overweight appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT00710814 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT00710814 about?

NCT00710814 is a clinical study titled "Trial of Leptin Administration After Roux-en-Y Gastric Bypass". This is a pilot and feasibility study to examine a novel intervention using leptin in weight-reduced individuals who have undergone bariatric surgery but still remain obese. Leptin, a peptide hormone secreted from adipose tissue, is a regulator of food intake and energy expenditure. Administration o...

What is the current status of trial NCT00710814?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2008-04. Estimated completion is 2014-07.

What conditions does trial NCT00710814 study?

This clinical trial studies the following conditions: Overweight.

What interventions are being tested in trial NCT00710814?

The interventions under investigation include: Placebo (OTHER), Leptin (DRUG).

Who is sponsoring clinical trial NCT00710814?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00710814 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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