ITMCTR2100004453RecruitingPhase 1
Clinical effect of herbal paste combined with Femoston to treat Premature ovarian insufficiency (POI)
Tongxiang Maternal and Child Health Hospital0 sitesStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 1
- Status
- Recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional study
Eligibility Criteria
- Ages
- 18 to 40 (—)
- Sex
- Female
Inclusion Criteria
- •1. Between 18 and 40 years of age;
- •2. Those who meet the diagnostic criteria of TCM and Western medicine;
- •3. Urine pregnancy test negative;
- •4. Those who did not receive any relevant treatment within 3 months prior to the start of the study;
- •5. Patients with informed consent and voluntary participation, can cooperate with the completion of clinical researchers.
Exclusion Criteria
- •1. Female reproductive system anatomical abnormalities;
- •2. In the past three months, the use of hormones, traditional Chinese medicine or acupuncture treatment;
- •3. Complicated with other gynecological reproductive endocrine diseases, such as endometriosis, hyper prolactinemia, polycystic ovary syndrome, gonadal dysplasia;
- •4. History of autoimmune diseases;
- •5. Patients with severe primary diseases, such as cardiovascular and cerebrovascular diseases, liver, kidney and hematopoietic system; Those who participated in other clinical trials at the same time did;
- •6. Not end or took other drugs that affected the study;
- •7. There are contraindications of acupuncture, such as large area of skin infection, rupture and so on;??
- •8. Not according to the prescribed medication, can not judge the efficacy, or incomplete data and other effects on the efficacy of the judge.
Investigators
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