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Post-marketing Safety and Efficacy Surveillance of Motherwort Injection

NCT06636422 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 20000

Last updated 2024-10-15

No results posted yet for this study

Summary

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

Conditions

  • Bleeding
  • Real-world Study
  • Adverse 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.

Sponsors & Collaborators

  • Zhong Wang

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-15
Primary Completion
2025-10-15
Completion
2025-10-15

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06636422 on ClinicalTrials.gov