Evaluation of Kisspeptin Glucose-Stimulated Insulin Secretion With Oral Glucose Tolerance Test
Completed · Phase 1 · Has a placebo group
Conditions studied: Metabolic Diseases
In brief
The goal of this study is to understand how exogenous kisspeptin affects metabolism by evaluating responses to an oral glucose tolerance test
Key facts
- Study ID
- NCT04958109
- Run by
- Massachusetts General Hospital
- People needed
- 16
- Starts
- 2021-10-28
- Expected to finish
- 2022-10-31
- Last updated by the study team
- 2026-03-06
Who can join
Age: 18 and older, up to 40. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- History:
- over the age of 18,
- normal pubertal development
- stable weight for previous three months,
- normal body mass index (BMI between 18.5-25)
- regular menstrual cycles
- Physical examination:
- systolic BP < 140 mm Hg, diastolic < 90 mm Hg
- Laboratory studies: (per Massachusetts General Hospital reference ranges)
- normal hemoglobin
- hemoglobin A1C < 6.5%
- blood urea nitrogen, creatinine not elevated
- aspartate aminotransferase, alanine aminotransferase < 3x upper limit of normal
You may not qualify if…
- active illicit drug use,
- history of a medication reaction requiring emergency medical care,
- difficulty with blood draws.
- history of chronic disease, except well controlled thyroid disease,
- recent use of prescription medications which interfere with metabolism or reproduction (recent = within 5 half-lives of the drug). Use of levothyroxine or seasonal allergy medications is acceptable,
- history of diabetes in a first degree relative,
- use of contraceptive pills, patches or vaginal rings within last 4 weeks.
- hyperlipidemia by fasting lipid panel
- positive serum pregnancy test (for all women)
Where it is running
- Massachusetts General Hospital — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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