Trials / Unknown
UnknownNCT06636422
Post-marketing Safety and Efficacy Surveillance of Motherwort Injection
Post-marketing Safety and Efficacy Surveillance of Motherwort Injection : a Registry Study
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 20,000 (estimated)
- Sponsor
- Zhong Wang · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
This study aims to provide evidence concerning the safety and efficacy of motherwort injection in real-world settings.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| 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. |
Timeline
- Start date
- 2024-10-15
- Primary completion
- 2025-10-15
- Completion
- 2025-10-15
- First posted
- 2024-10-10
- Last updated
- 2024-10-15
Source: ClinicalTrials.gov record NCT06636422. Inclusion in this directory is not an endorsement.