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Centralized monitoring study for safety of Traditional Chinese Medicine granules

A multi-centre, prospective, open-lable, observational study for monitoring the safety of Traditional Chinese Medicine granules

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000031605
Enrollment
Unknown
Registered
2020-04-05
Start date
2020-04-07
Completion date
Unknown
Last updated
2022-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

adverse drug reaction

Interventions

Sponsors

First Affiliated Hospital of Guang zhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who will take TCM granules, which prescribed by the doctor; 2. Patients who participate in this study voluntarily.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
The occurrence of adverse drug reaction;

Secondary

MeasureTime frame
The occurrence of adverse event;The occurrence of serious adverse event;The occurrence of serious adverse drug reaction;

Countries

China

Contacts

Public ContactYang Zhongqi

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

yang_zhongqi@163.com+86 13688867618

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026