ITMCTR2200005690
Not yet recruiting
Phase 1
A randomized controlled study of the effect of electro-acupuncture on endometrial blood flow in RIF patients
Chengdu Xinan Gynecological Hospital0 sitesTBD
Conditionsrecurrent implantation failure
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- recurrent implantation failure
- Sponsor
- Chengdu Xinan Gynecological Hospital
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Aged between 22 to 40 female.
- •(2\) Meeting the diagnostic criteria for recurrent implantation failure.
- •(3\) The availability of frozen embryos and prepare for FET .
- •(4\) Patients undergoing endometrial preparation using a hormone replacement therapy or Gnrh\-a down regulation hormone replacement therapy.
- •(5\)Patients with endometrial flow type II or type I.
- •(6\) Signed an informed consent form.
- •Note: Patients meeting all 6 criteria above were included in this study.
Exclusion Criteria
- •(1\) Ultrasound examination shows unaddressed uterine malformations that clearly affect uterine morphology, uterine fibroids that compress the uterine cavity, or ovarian cysts
- •(2\) Having a clearly diagnosis autoimmune disease or pre\-thrombotic state, such as systemic lupus erythematosus, rheumatoid arthritis, etc.
- •(3\) Having an unsolved endocrine disorder, such as hyperthyroidism, diabetes mellitus, hypertension, etc.
- •(4\) Suffering from a clearly diagnosed medical or surgical serious primary or secondary disease or psychiatric disorder in progress.
- •(5\) Patients with chromosomal abnormalities(Except for chromosome polymorphism).
- •(6\) The patient has a history of assisted reproduction live births
- •(7\) Patients with bleeding tendencies and those prone to infection, or those suffering from severe allergies, or with skin ulcers or scarring that prohibit needling or dizziness.
- •(8\) Patients who have received acupuncture treatment in the last three months.
- •(9\) Patients who are participating in other clinical trials.
- •Note: Anyone who meets any 1 of the above criteria will be excluded.
Outcomes
Primary Outcomes
Not specified
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