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Kisspeptin to Quantify GnRH Neuronal Function in Health and Disease

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: f
View:

• Female (ages 18-45 years) or Male (ages 18-60 years)

• No current or recent use of a medication (including hormonal replacement) that, in the opinion of a study investigator, can modulate the reproductive axis or willing to complete an appropriate washout for that particular medication and its method of administration

• For women, negative serum hCG pregnancy test

• For cases, diagnosis of post-covid-19 syndrome

• For controls, history of prior covid infection but no diagnosis of post-covid-19 syndrome

Locations
United States
Massachusetts
Massachusetts General Hospital
RECRUITING
Boston
Contact Information
Primary
Study Coordinator
MGHKisspeptinResearch@partners.org
617-643-2308
Time Frame
Start Date: 2026-03-10
Estimated Completion Date: 2030-05
Participants
Target number of participants: 40
Treatments
Experimental: Kisspeptin administration
Single bolus of kisspeptin
Related Therapeutic Areas
Sponsors
Leads: Stephanie B. Seminara, MD
Collaborators: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

This content was sourced from clinicaltrials.gov