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Study identifier: NCT06414096 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Use of Pulsatile Intravenous FSH to Mitigate Reprometabolic Syndrome

Condition: Infertility · Obesity  ·  Sponsor: University of Colorado, Denver

PhasePhase 1
Planned participants5
Who can joinFemale, 19 Years to 37 Years
Healthy volunteersYes

About this study

Hypothesis: The investigators hypothesize that pulsatile FSH intravenous administration to women with obesity will correct the Reprometabolic Syndrome (RMS) luteal deficiency phenotype. Specific Aim: To test the hypothesis that pulsatile IV administration of FSH will rescue the impaired folliculogenesis and relative hypogonadotropic hypogonadism, characteristic of obesity. The investigators will accomplish this by administering a cycle of pulsatile FSH to women with obesity and comparing their hormone output to a cycle using conventional, daily FSH injection at the identical daily dose. The primary outcome will be luteal phase progesterone excretion.

This description comes directly from the study's public registry record.

Talk to the study team

Katherine Kuhn, MS  ·  303-7245276  ·  Katherine.Kuhn@cuanschutz.edu

Asma Giornazi, MS  ·  303-724-5276  ·  Asma.Gioranzi@ucdenver.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Colorado Anschutz Medical CampusAurora, Colorado, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06414096