| Registry | NCT06583408, acronym REVEAL |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Enrollment | 100000 (Estimated) |
| Sponsor | Mayo Clinic (Other) |
| Conditions | Hypothalamic Amenorrhea, Functional, Hypothalamic Amenorrhea, Functional Hypogonadotropic Hypogonadism |
| Interventions | Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24), REVEAL Questionnaire (Other) |
| Dates | start 2024-07-01, primary completion 2029-08-01 (estimated), completion 2029-08-01 (estimated), first posted 2024-09-04, last updated 2025-11-21 |
| Locations | 2 sites in United States |
Related Papers Related Patents Related Grants Related Experts
All trials for Hypothalamic Amenorrhea, Functional All trials for Hypothalamic Amenorrhea All trials of Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24) All trials of REVEAL Questionnaire
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.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Women with > 3 months amenorrhea | Other: Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24); Other: REVEAL Questionnaire | Women aged 18-40 years old with a diagnosis of functional hypothalamic amenorrhea, or lab results that are within the inclusion criteria. |
Sex: Female, ages: 18 Years to 40 Years
Inclusion Criteria: * 3 or more months of consecutive amenorrhea with a diagnosis of functional hypothalamic amenorrhea or screening hormones consistent with functional hypothalamic amenorrhea including but not limited to: * Estradiol: < 50pg/mL * LH: < 10 IU/mL * FSH: < 10 IU * Testosterone: 2 - 45 ng/dL * Free Testosterone: 0.1 - 6.4 pg/mL * FT4: 0.93 - 1.70 ng/dL * Prolactin: < 20 ng/mL * AMH: > 1 ng/mL * Urine or serum human chorionic gonadotropin: Negative * LH:FSH Ratio <1 * No signs of male-like hair growth on the upper lip, chin, chest, abdomen, buttocks, or back * Does not have a diagnosis for secondary amenorrhea, including prolactinoma, PCOS, premature ovarian insufficiency, pituitary surgery, infection, or infarction * Premenopausal status determined by WISE criteria * Able to give informed consent * Able to read English Exclusion Criteria: * Parturition/lactating in the last 6-12 months * Lack of consent
| Facility | City | Country | Status |
|---|---|---|---|
| Mayo Clinic | Jacksonville, Florida | United States | Recruiting |
| Mayo Clinic | Rochester, Minnesota | United States | Recruiting |