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Effect of Zishen Yufei wan in women with unexplained recurrent abortion: a randomized controlled double-blind clinical study

Effect of Zishen Yufei wan in women with unexplained recurrent abortion: a randomized controlled double-blind clinical study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065326
Enrollment
Unknown
Registered
2022-11-02
Start date
2022-11-02
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

unexplained recurrent abortion

Interventions

Control:Dydrogesterone + placebo
Intervention group:Dydrogesterone + Zishen Yufei wan

Sponsors

Chongqing Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 42 Years

Inclusion criteria

Inclusion criteria: 1. Aged 20-40 years; 2. Spontaneous abortion >= 2 consecutive times with the same partner; 3. Patients and their family members fully understood the content of the study and voluntarily signed informed consent; 4. Gestational age < 8 weeks.

Exclusion criteria

Exclusion criteria: 1. Chromosomal abnormalities in embryos of either spouse; 2. Thrombolysis; 3. Uncured uterine anatomical abnormalities, including uterine congenital malformations, cervical insufficiency, intrauterine adhesions, uterine fibroids, etc.; 4. Fetal abnormality; 5. Allergic to or was prohibited by known drug ingredients; 6. Bleeding caused by vaginal and cervical factors; 7. Suffering from serious organic lesions of the heart, liver, kidney or brain, and serious physical diseases or malignant tumors; 8. BMI >= 30 kg/m2; 9. With autoimmune diseases that have been identified to be associated with recurrent abortion; 10. Had used hormone drugs one month before randomization, and had taken other kidney tonifying Chinese patent medicine or traditional Chinese medicine decoction one month before randomization; 11. Endocrine diseases, such as hyperlactatemia, thyroid diseases, diabetes mellitus, polycystic ovary syndrome, etc.; 12. The investigator did not consider it appropriate to participate in the trial.

Design outcomes

Primary

MeasureTime frame
live birth rate;

Countries

China

Contacts

Public ContactHao Lijuan

Chongqing Maternal and Child Health Hospital

haolj2002@163.com+86 13002357880

Outcome results

None listed

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