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Clinical trial

Post-marketing Safety and Efficacy Surveillance of Motherwort Injection : a Registry Study

NCT06636422 is registered in ClinicalTrials.gov with Zhong Wang as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Post-marketing Safety and Efficacy Surveillance of Motherwort Injection : a Registry Study
Lead sponsor
Zhong Wang
Phase
Observational
Overall status
Unknown status
Start date
October 15, 2024
Completion date
October 15, 2025
Enrollment
20,000 (estimated)
Sites
Not reported

Conditions

As the registry lists them; a condition with its own page is linked.

adverse events, bleeding, real-world study