Does Spironolactone Normalize Sleep-wake Luteinizing Hormone Pulse Frequency in Pubertal Girls With Hyperandrogenism?

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexFemale
Age10-17
SponsorUniversity of Virginia

About this trial

The purpose of this study is to determine if, in mid- to late pubertal girls with hyperandrogenism (HA), androgen-receptor blockade (spironolactone) alone normalizes sleep-wake luteinizing hormone (LH) pulse frequency (primary endpoint) and overall LH and follicle-stimulating hormone secretion (secondary endpoints).

Eligibility criteria

Qualifiers

Mid- to late pubertal adolescent girls as signified by either (a) post-menarcheal status (Tanner breast stages 2-5) or (b) Tanner breast stage of 4 or 5 (whether pre-menarcheal or post-menarcheal) ages 10-17 years.

Hyperandrogenism, defined as a serum (calculated) free testosterone concentration greater than the Tanner stage-specific reference range and/or clinical hirsutism

General good health (excepting obesity, hyperandrogenism, PCOS, and adequately-treated hypothyroidism)

Willing to strictly avoid pregnancy with use of reliable non-hormonal methods during the study period.

Disqualifiers

Inability/incapacity to provide informed consent

Males will be excluded (hyperandrogenism is unique to females)

Age < 10 or > 17 years (this study is designed to elucidate mechanisms underlying emerging PCOS in mid- to late pubertal adolescent girls

Post-menarcheal by > 4 years

Trial design

Treatments tested in this trial

  • Spironolactone
  • Placebo

Treatment groups

32 Participants
are divided into 2 treatment groups

Locations

1
Center for Research in Reproduction, University of Virginia22908, CharlottesvilleVirginia, United States

Sponsors and collaborators

University of Virginia

Lead sponsor

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator