Kisspeptin to Quantify GnRH Neuronal Function in Health and Disease
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Stephanie B. Seminara, MD
- Study ID
- NCT07224490
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Long COVID
- Neurodegeneration
- Reproductive Disorder
- SARS-CoV 2
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 60 Years
- Healthy Volunteers
- Not accepted
Interventions
- Kisspeptin 112-121 — DRUGSingle bolus of kisspeptin
Study Details
The objective of this protocol is to use a case-control paradigm to compare the response to an intravenous administration of kisspeptin in individuals with and without post-covid-19 syndrome. The study subjects will receive a single bolus of kisspeptin. This study will utilize the technique of frequent blood sampling (q10 minutes) to provide detailed neuroendocrine characterization of endogenous LH secretion before and after kisspeptin administration. This frequency of blood sampling is required to define the features of LH pulses.
Key Dates
- Start date
- Mar 10, 2026
- Status verified
- Mar 2026
- Primary completion
- May 31, 2030
- Completion
- May 31, 2030
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- OTHER
Arms
- Experimental: Kisspeptin administrationSingle bolus of kisspeptin
Primary Outcome Measure
Difference in mean luteinizing hormone (LH) amplitude between cases and controls [ Time Frame: Day of study visit (one to two hours) ]
Central Contacts
- Study Coordinator617-643-2308
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Massachusetts General Hospital | Boston | Massachusetts | 02114 |
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