Centralized monitoring study for safety of Traditional Chinese Medicine granules
Phase 4
Recruiting
- Conditions
- adverse drug reaction
- Registration Number
- ITMCTR2000003180
- Lead Sponsor
- First Affiliated Hospital of Guang zhou University of Chinese Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
1. Patients who will take TCM granules, which prescribed by the doctor;
2. Patients who participate in this study voluntarily.
Exclusion Criteria
1. Patients who won't take TCM granules;
2. Non-compliant patients who won't cooperate with follow-up visit;
3. Patients who have participated in this study;
4. Lactating or pregnant women, planning for pregnancy, male or female who lacking effective contraception during the study;
Study & Design
- Study Type
- Observational study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The occurrence of adverse drug reaction;
- Secondary Outcome Measures
Name Time Method The occurrence of adverse event;The occurrence of serious adverse event;The occurrence of serious adverse drug reaction;