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Clinical study of Bushen Huoxue Prescription on treatment mechanism and progeny of unexplained recurrent abortion

A randomized, double-blind, controlled trial of Bushen Huoxue prescription in the treatment of sliding fetus with kidney deficiency and blood stasis syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069777
Enrollment
Unknown
Registered
2023-03-24
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Unexplained Recurrent Spontaneous Abortion

Interventions

Bushen Huoxue prescription combined with aspirin group:Bushen Huoxue prescription combined with aspirin for 3 months
Bushen Huoxue formula combined with aspirin placebo group:Bushen Huoxue prescription combined with aspirin placebo treatment for 3 months
Bushen Huoxue formula placebo combined with aspirin group:Bushen Huoxue prescription placebo combined with aspirin
Bushen Huoxue prescription placebo combined with aspirin placebo group:Bushen Huoxue prescription placebo combined with aspirin placebo was administered for 3 months

Sponsors

The First Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Women of childbearing age, aged 20-40 years; (2) Normal menstrual cycle (28~30 days); (3) Urine pregnancy test is negative, blood ß-HCG < 5IU/L, consent to use contraceptives during the medication; (4) The diagnostic criteria of URSA Western medicine and syndrome of kidney deficiency and blood stasis of slippery fetus were met; (5) Sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with a clear cause of RSA; (2) The male etiology is clearly abnormal; (3) complicated with other diseases (such as diabetes mellitus, neoplasms, digestive diseases, heart, liver, kidney, blood system diseases and neuropsychiatric diseases); (4) genital tract abnormalities and endocrine abnormalities; (5) Clear trauma, ovulation disorders, fallopian tube obstruction and other effects of re-conception; (6) Recent history of exposure to parasitic infections and harmful poisons. (7) pregnant and lactating women; (8) Those who have recently taken other medium (adult) drugs or taken hormone drugs within three months; (9) Those who cannot take the medicine on time for other reasons; (10) Patients participating in other clinical trials; (11) The researchers felt that other reasons were not appropriate for clinical trials.

Design outcomes

Primary

MeasureTime frame
Factors associated with angiogenesis;Factors associated with iron death;

Secondary

MeasureTime frame
Coagulation index;Uterine arterial blood perfusion;Safety index;

Countries

China

Contacts

Public ContactXiaoling Feng

The First Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine

doctorfxl@163.com13604800585

Outcome results

None listed

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