Clinical study on infertility caused by premature ovarian insufficiency treated with mili-fire needle syndrome differentiatio

Not Applicable

Recruiting

• Conditions: Premature Ovarian insufficiency

• Registration Number: ITMCTR2100004971
• Lead Sponsor: anjing Hospital of Traditional Chinese Medicine Affiliated Hospital of Nanjing University of Traditional Chinese Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

1. According to the diagnosis of infertility caused by early ovarian function in western medicine and the syndrome differentiation of traditional Chinese medicine, patients with kidney deficiency;
2. Women aged 24 to 40 years;
3. Men with normal reproductive function;
4. Anti-muller hormone AMH 1.1 to 2ng/ml;
5. The number of sinus follicles AFC < 4;
6. Agreed to receive treatment according to this program and follow up observers;
7. Willing to sign informed consent;
8. Willing to register a case.

Exclusion Criteria

1. Women in pregnancy or menopause at the time of consultation;
2. Organic lesions causing POI were confirmed by conventional gynecological examinations, such as imaging examination and secretion examination;
3. Have received the relevant treatment and may affect the effect observation indicators;
4. Severe heart, liver and kidney injuries affect normal drug metabolism;
5. The combination of other physiological or pathological states that may affect the effect indicators;
6. Withdrawal from treatment due to personal reasons;
7. Failure to strictly implement the intervention measures and change the treatment plan leads to failure to collect or produce errors in relevant data such as feedback of efficacy and effect indicators;
8. Severe adverse reactions and complications occur during treatment, and they are unable to continue treatment;
9. Use of drugs that interfere with the treatment plan;
10. Participate other experimenters at the same time;
11. Unable to complete the filling of various scales;
12. Unwilling to be randomly grouped;
13. Patients with abnormal thyroid function.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
sex hormone;B ultrasound imaging monitoring and evaluation;Oxidative stress index;

Secondary Outcome Measures

Name	Time	Method
Clinical Correlation Scale;The pregnancy rate;