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NCT06610162 · ClinicalTrials.gov registry record · NA
Thermogenenic Responses to Fasting and Overfeeding in Women
A NA study of Obesity, sponsored by University of Colorado, Denver.
- Recruiting
- Registry status
- NA
- Development phase
- 56
- Enrollment target
- 1
- Study location
NCT06610162 is a NA study of Obesity that is actively recruiting participants, run by University of Colorado, Denver. The registered enrollment target is 56 participants, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06610162, a NA study of Obesity, is actively recruiting participants, sponsored by University of Colorado, Denver.
- RECRUITING
- Registry status
- NA
- Development phase
- 56 participants
- Enrollment target
- 1
- Study location
Study Summary
This study plans to learn more about why menopause increases the risk of weight gain. During and after menopause, women are prone to increased weight gain. The weight gained is primarily body fat, particularly visceral or abdominal body fat. The excess gain in abdominal fat during menopause increases the risk of chronic metabolic diseases such as heart disease and diabetes. The increase in weight and body fat with menopause may be due to changes in metabolism related to the loss of estrogen. This study plans to compare how the metabolism of premenopausal and postmenopausal women responds to changes in energy intake. The investigators will compare the changes in energy expenditure that occur during a period of acute fasting (24 hours) and a period of consuming excess calories (overfeeding).
Conditions Studied
Interventions
- OTHER Eucalaloric feeding
- OTHER Acute Fasting
- OTHER Acute Overfeeding
Study Locations (1)
Colorado
- University of Colorado Anschutz Medical Campus - Aurora
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 56 participants |
| Start Date | 2025-01-01 |
| Est. Completion | 2030-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06610162
The ClinicalTrials.gov registry entry for NCT06610162 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 56 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (93% lower). The listed sponsor is University of Colorado, Denver, which has 1,283 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Obesity appearing as the primary indexed condition, and to 3 interventions - of which Eucalaloric feeding is the first listed.
NCT06610162 reports 1 study location spanning 1 distinct geographic area - top geographies include Colorado.
Frequently Asked Questions
What is clinical trial NCT06610162 about?
NCT06610162 is a clinical study titled "Thermogenenic Responses to Fasting and Overfeeding in Women". This study plans to learn more about why menopause increases the risk of weight gain. During and after menopause, women are prone to increased weight gain. The weight gained is primarily body fat, particularly visceral or abdominal body fat. The excess gain in abdominal fat during menopause increase...
What is the current status of trial NCT06610162?
This trial is currently recruiting. It is a NA study. The enrollment target is 56 participants. The study started on 2025-01-01. Estimated completion is 2030-12-31.
What conditions does trial NCT06610162 study?
This clinical trial studies the following conditions: Obesity.
What interventions are being tested in trial NCT06610162?
The interventions under investigation include: Eucalaloric feeding (OTHER), Acute Fasting (OTHER), Acute Overfeeding (OTHER).
Who is sponsoring clinical trial NCT06610162?
This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06610162 being conducted?
This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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