Post-marketing Safety and Efficacy Surveillance of Motherwort Injection
NCT ID: NCT06636422
Last Updated: 2024-10-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
20000 participants
OBSERVATIONAL
2024-10-15
2025-10-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients indicated for Motherwort injection
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.
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.
Interventions
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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.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Voluntarily participate in this study
* Fulfill ethical requirements.
Exclusion Criteria
ALL
No
Sponsors
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Zhong Wang
OTHER
Responsible Party
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Zhong Wang
Sponsor
Central Contacts
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Other Identifiers
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Motherwort-V2.0
Identifier Type: -
Identifier Source: org_study_id
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