A randomized controlled trial of acupuncture on subclinical premature ovarian insufficiency
- Conditions
- premature ovarian insufficiency
- Registration Number
- ITMCTR2100004761
- Lead Sponsor
- the Third Affiliated Hospital of Zhejiang Chinese Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- Not specified
1. Female patients aged between 25-40 years;
2. Havent received any other treatments in the last two months before enrollment;
3. Patients voluntarily participate in the study;
4. Sign the informed consent form.
1. Those who are pregnant or have a pregnancy plan in six months;
2. Patients with primary amenorrhea;
3. Congenital reproductive organ abnormalities;
4. Patients with internal diseases which can affect reproductive hormones, such as thyroid disease, SLE, etc.;
5. Patients with other serious internal diseases and mental diseases;
6. Patients with unilateral or bilateral oophorectomy;
7. Those who are unable to tolerate the tests or treatments during the course of this study;
8. Those who are participating in other clinical trials.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method follicle stimulating hormone, FSH;anti-Mullerian hormone, AMH;
- Secondary Outcome Measures
Name Time Method Menstrual condition;FSH/LH;estradiol E2, E2;Kupperman index;Luteinizing hormone, LH;