A multi-center real-world study for the application of Motherwort injection in the field of family planning after market

Phase 4

Recruiting

• Conditions: Abortion, placement or removal of an IUD

• Registration Number: ITMCTR2000004159
• Lead Sponsor: He'nan Provincial People's Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

1. After induced abortion
Women of childbearing age who were diagnosed with pregnancy and required abortion were selected as the subjects of the study. And meet the following criteria:
1) Women eligible for induced abortion;
2) Aged18-40 years old, in good health in the past;
3) Can fill in the bleeding card;
4) Volunteer for the study.
(2) After placing the IUD
Women of childbearing age who were selected for IUD placement were studied. And meet the following criteria:
1) If the IUD is selected and placed as a long-term contraceptive method, or vaginal bleeding >=8 days after the PLACEMENT of the IUD;
2) Can fill in the bleeding card;
3) Volunteer to participate in the study and sign the informed consent.
(3) After the IUD is removed
Healthy women who had their IUDs removed were selected and studied for reasons such as pregnancy or menopause. And meet the following criteria:
1) Patients aged between 20 and 65 who voluntarily take the ring without surgical contraindications;
2) Can fill in the bleeding card;
3) Volunteer to participate in the study and sign the informed consent.

Exclusion Criteria

1) Allergy to this product or excipients listed in motherwort preparation and ingredients or history of serious adverse reactions;
2) Patients with allergic constitution (allergic to motherwort or to motherwort preparation) + pregnant women;
3) Patients whom the researcher considers inappropriate.

Study & Design

• Study Type: Observational study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
menstruation recovery time;vagina bleeding time;