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A diminished ovarian reserve prediction cohort study

Not Applicable
Conditions
Tracking of menstrual cycles and prediction of diminished ovarian reserve via wearable devices
Urological and Genital Diseases
Registration Number
ISRCTN27534184
Lead Sponsor
Obstetrics and Gynecology Hospital of Fudan University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
Female
Target Recruitment
120
Inclusion Criteria

1. Aged 18-45 years old
2. AMH < 1.1 ng/mL
3. Menstruation within at least 6 months
3. Willing to participate in the follow-up and sign the informed consent

Exclusion Criteria

1. Menopause, pregnancy, lactation
2. Exogenous hormones within 3 months, history of ovarian surgery, planned exogenous hormone therapy
3. Suffering from other states or diseases that can affect heart rate, respiration, body temperature and sleep parameters: diseases of the cardiovascular system (hypertension, heart disease, arrhythmia, wearing a pacemaker, etc.), respiratory diseases, abnormalities of the thyroid function (hyperthyroidism/hypothyroidism, positive antibodies are not excluded), taking psychotropic medications
4. Severe systemic disease or any unstable disease or medical condition that, according to medical criteria, may jeopardize patient safety and his/her compliance with the requirements of the study

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fertility measured using a serum anti-mullerian hormone (AMH) blood test at baseline, which is determined on the 2nd-4th day of menstruation for patients with a regular menstrual cycle, and on any day for those with irregular menstrual cycle
Secondary Outcome Measures
NameTimeMethod
Fertility measured using a basal hormone blood test (FSH, LH, E2, P, PRL, T, DHEA) at baseline and > 4 weeks, which is determined on the 2nd-4th day of menstruation for patients with regular menstrual cycle, and on any day for those with irregular menstrual cycle
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