Post-marketing Safety and Efficacy Surveillance of Motherwort Injection

Not yet recruitingOBSERVATIONAL
Enrollment

20,000

Participants

Timeline

Start Date

October 15, 2024

Primary Completion Date

October 15, 2025

Study Completion Date

October 15, 2025

Conditions
BleedingReal-world StudyAdverse Events
Interventions
DRUG

Motherwort injection

Patients will be given motherwort injection according to their disease condition in the real world. The investigator only can record the information on the usage of the drug and the relevant medications without any interventions.

All Listed Sponsors
lead

Zhong Wang

OTHER

NCT06636422 - Post-marketing Safety and Efficacy Surveillance of Motherwort Injection | Biotech Hunter | Biotech Hunter