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 — DRUG
    Single 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 administration
    Single 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

Locations (1)

FacilityCityStateZIPSite coordinators
Massachusetts General HospitalBostonMassachusetts02114
Study Coordinator
617-643-2308

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