Randomized controlled application of motherwort injection in artificial abortion

Postoperative uterine instauration of leonurus injection to promote abortion multicenter randomized controlled clinical studies

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-15006621

Enrollment

Unknown

Registered

2015-06-18

Start date

2015-06-03

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Bleeding after abortion

Interventions

Leonurus injection group:Intramuscular injection of leonurus injection

Blank control group:blank control group

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1) comply with the gestational age and within 10 weeks after surgery in painless abortion women; 2) ages between 18 to 40 years old, always in good health; 3) agreed to participate in the test and sign the informed consent will be.

Exclusion criteria

Exclusion criteria: 1) allergic constitution; 2) abortion intraoperative bleeding is more, greater than 100 ml; 3) combined with uterine fibroids and scar uterus; 4) patients not to cooperate, not willing to sign the informed consent will be.

Design outcomes

Primary

Measure	Time frame
amount of bleeding;	—

Secondary

Measure	Time frame
B-type ultrasonic;bleeding time;	—

Countries

China

Contacts

Public ContactQian Zeng

zqian999d@126.com+86 18981885627

Outcome results

None listed

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