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A Randomized Controlled Study for the Treatment of Endometriosis Infertility

A Randomized Controlled Study for the Treatment of Endometriosis infertility

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022489
Enrollment
Unknown
Registered
2019-04-13
Start date
2019-05-01
Completion date
Unknown
Last updated
2019-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis Infertility

Interventions

treatment group:Neiyi compound recipe+Medroxyprogesterone Acetate Tablets+IVF-ET
control group:Placebo+Medroxyprogesterone Acetate Tablets+IVF-ET

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) All cases must meet the diagnostic criteria of infertility. (2) All cases should conform to EM pathological diagnostic criteria and diagnostic criteria of kidney deficiency and blood stasis. (3) All cases should meet the baseline criteria: age 25-40, normal menstrual cycle (21-35 days). And on the third day of menstruation, bilateral sinus follicles (AFC) < 5, 10 < FSH < 25 mIU/ml, AMH 0.5ng/ml-1.1ng/ml. (4) Those who volunteered to participate in the experiment and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Failure to meet the diagnostic criteria for infertility. (2) Infertility caused by other reasons, such as tubal infertility, immune infertility and male factor infertility, does not meet the EM diagnostic criteria. (3) It does not meet the diagnostic criteria of kidney deficiency and blood stasis.

Design outcomes

Primary

MeasureTime frame
Clinical pregnancy rate;

Secondary

MeasureTime frame
medicine;number of embryos transferred;embryo implantation rate;Differential expression of inflammatory factors in follicular fluid;Symptom record;

Countries

China

Contacts

Public ContactChaoqin Yu

Shanghai Changhai Hospital

chqyu81@163.com+86 13818390984

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026