Hypothalamic Amenorrhea

5

Review clinical trials related to Hypothalamic Amenorrhea. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Kisspeptin Administration Subcutaneously to Patients With Hypothalamic Amenorrhea

The goal of this study is to see whether kisspeptin, a naturally occurring hormone, can stimulate the release of other reproductive hormones in women with hypothalamic amenorrhea (HA). The investigators are also examining whether kisspeptin can help women release eggs from their ovaries. Kisspeptin will be administered subcutaneously (SC) for two weeks in a pulsatile fashion. Ultrasound monitoring of ovarian follicular growth and frequent blood sampling (every 10 minutes for up to two hours) will be performed to assess the physiologic response to kisspeptin over time.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Stephanie B. Seminara, MDUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Female [+7]

Any condition (medical, mental, or behavioral) that, in the opinion of a study i... [+6]

Status: Recruiting

Kisspeptin Administration Subcutaneously to Patients With Hypothalamic Amenorrhea

The goal of this study is to see whether kisspeptin, a naturally occurring hormone, can stimulate the release of other reproductive hormones in women with hypothalamic amenorrhea (HA). The investigators are also examining whether kisspeptin can help women release eggs from their ovaries. Kisspeptin will be administered subcutaneously (SC) for two weeks in a pulsatile fashion. Ultrasound monitoring of ovarian follicular growth and frequent blood sampling (every 10 minutes for up to two hours) will be performed to assess the physiologic response to kisspeptin over time.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Stephanie B. Seminara, MDUpdated: Dec 31, 2025Locations: 1
Eligibility criteria

Female [+7]

Any condition (medical, mental, or behavioral) that, in the opinion of a study i... [+6]

Status: Recruiting

The REgistry of Very Early Estrogen and AnovuLation

The purpose of this study is to to build a registry of women with early estrogen loss due to Functional Hypothalamic Amenorrhea (FHA) to understand the prevalence, racial and ethnic diversity of this condition.

Participants needed: 100,000
Trial details
Age: 18-40Biological sex: FemaleType: ObservationalSponsor: Mayo ClinicUpdated: Nov 21, 2025Locations: 2Duration: 5 Years
Eligibility criteria

Estradiol: < 50pg/mL [+14]

Parturition/lactating in the last 6-12 months [+1]

Status: Recruiting

Body Fat as Determinant of Female Gonadal Dysfunction

Reproduction requires from women enough energy depots to warrant an adequate nutritional supply to the fetus. Hence, adipose tissue is able to communicate with female hypothalamic-pituitary-ovary axis. The hypothesis of the project is that abnormalities in the quantity (absolute and relative to lean body mass), distribution and/or function of adipose tissue are associated with functional forms of female gonadal dysfunction in predisposed women, in a spectrum of anomalies that go from hypothalamic amenorrhea to the polycystic ovary syndrome (PCOS). To challenge this hypothesis, the investigators will study 5 groups of 10 women each: women with exercise-associated hypothalamic amenorrhea, women without ovulatory dysfunction that exercise equally, non-hyperandrogenic patients with PCOS, hyperandrogenic patients with PCOS, and healthy control women comparable to those with PCOS. The aims of the study will be: Primary objective: To identify novel signalling factors originating from adipose tissue and muscle using targeted and nontargeted evaluation of the proteome and of gene expression of superficial subcutaneous fat, deep subcutaneous fat (which mimics visceral adipose tissue) and skeletal muscle. Secondary objectives: 1. To study the serum adipokine profile - including those identified by the primary objective - and circulating gut hormones during fasting and after a glucose load in the 5 groups of women, and their associations with sexual hormones and body fat distribution. 2. To study body composition and body fat distribution in these women and their relationships with: 2.1, Sex steroid profiles. 2.2. Classic cardiovascular risk factors: carbohydrate metabolism, lipid profiles and blood pressure. 2.3 Markers of low-grade chronic inflammation. 2.4. Oxidative stress markers. 2.5. Cardiovascular autonomic function. 2.6. Surrogate markers of subclinical atherosclerosis. 2.7. Circulating concentrations of endocrine disruptors. 2.8. Oral and gut microbiome. The results will provide a better understanding of the mechanisms linking body energy depots with the female reproductive axis and, hopefully, the identification of potential biomarkers for the diagnosis and treatment of the disorders studied here.

Participants needed: 50
Trial details
Age: 18-40Biological sex: FemaleType: ObservationalSponsor: Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y CajalUpdated: Aug 12, 2025Locations: 1
Eligibility criteria

Body mass index between 18.5 and 25.0 kg/m2. [+21]

Oral drugs interfering with ovulation (glucocorticoids, antipsychotics, antidepr... [+4]