Post-marketing Safety and Efficacy Surveillance of Motherwort Injection

Zhong Wang

Status: Not yet enrolling

Conditions: Adverse Events; Real-world Study; Bleeding

Treatments: Drug: Motherwort injection

Study type: Observational

Funder types: Other

Identifiers

NCT06636422

Motherwort-V2.0

Details and patient eligibility

About

This study aims to provide evidence concerning the safety and efficacy of motherwort injection in real-world settings.

Enrollment: 20,000 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Meet the clinical indications for the use of motherwort injection
• Voluntarily participate in this study
• Fulfill ethical requirements.

Exclusion criteria

• None

Trial design

20,000 participants in 1 patient group

Patients indicated for Motherwort injection

Description:

During the registration and enrollment period of the study, all patients who meet the clinical indications for the use of motherwort injection, as determined by the physician, and voluntarily agree to participate while fulfilling ethical requirements, will be recruited from designated medical institutions and departments. The observation period for each observer was established based on the clinical application of motherwort injection.

Treatment:

Drug: Motherwort injection