View Clinical Trial (Medical Research Study)
Trial of Leptin Administration After Roux-en-Y Gastric Bypass - NCT00710814-10032(Clinical Trial 230209)
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New York |
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State:
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NY |
| Zip Code: |
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10032 |
| Conditions: |
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Overweight |
| Purpose: |
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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. We 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.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- Women only.
- Must have had Roux-en-Y gastric bypass 18 months to 10 years ago.
- Current BMI between 28 to 44.
- Must live in the vicinity of New York City to comply with 11 study visits over 34
weeks.
- Must be willing to self-inject study drug twice per day.
Exclusion Criteria:
- Diabetes.
- History of plastic surgery. |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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January 5, 2011 |
Modifications to
this listing: |
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