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Clinical Trials/ITMCTR2200005907
ITMCTR2200005907
Not yet recruiting
Phase 1

A randomized controlled trial of acupuncture in the treatment of ovarian reserve dysfunction

Chengdu Xinan gynecological hospital0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
ovarian reserve dysfunction
Sponsor
Chengdu Xinan gynecological hospital
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Female

Investigators

Sponsor
Chengdu Xinan gynecological hospital

Eligibility Criteria

Inclusion Criteria

  • (1\) 20 years \= age \< 40 years;
  • (2\) Meet the diagnostic criteria of ovarian reserve dysfunction;
  • (3\) Voluntarily participate in the trial and sign the informed consent form.

Exclusion Criteria

  • (1\) Patients suffering from severe systemic organic diseases such as heart, liver and kidney, which makes it difficult to achieve pregnancy;
  • (2\) Combined with congenital reproductive organ development abnormalities affecting pregnancy, endometrial polyps, hysteromyomas, endometriosis, or other organic diseases.
  • (3\) Patients with polycystic ovary syndrome, hyperprolactinemia, hyperandrogenemia, hypothyroidism, chronic adrenocortical dysfunction and other diseases;
  • (4\) Severe wasting disease or developing malignant tumor;
  • (5\) Patients with bleeding tendency and prone to infection, or patients with severe allergies, or patients with skin ulcers, scars and other prohibited acupuncture;
  • (6\) IVF\-ET planners are expected within 2 months after enrollment.
  • Note: patients who meet any of the above conditions should be excluded.

Outcomes

Primary Outcomes

Not specified

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