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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03189199
Other study ID # RSCMI-12
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 14, 2017
Last updated June 18, 2017
Start date June 19, 2017
Est. completion date December 31, 2019

Study information

Verified date June 2017
Source China Academy of Chinese Medical Sciences
Contact Yan Ming Xie, BA
Phone 0086-13521781839
Email datamining5288@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to make a cohort event monitoring to see whether and how Dazhuhongjingtian injection in hospital results in adverse events or adverse drug reactions


Description:

Safety surveillance on Chinese Medicine injection is an important problem that needs to be sorted out ,because in mainland China hospitals ,Chinese Medicine Injection are used widely. Population for taking medicine characteristics,the incidence rate of ADR and other uncertain factors influence can few be found now.A registry study for Dazhuhongjingtian injection safety surveillance with 3000 patients will be conducted from June.2017 to Dec.2019.Eligibility criteria Patients who will use Dazhuhongjingtian injection in 4 selected hospitals from2017-2019.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 3000
Est. completion date December 31, 2019
Est. primary completion date July 19, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- An anticipated sample size was caculated in this study, about 3000. Patients using Dazhuhongjingtian injection from 2017 to 2019 in 4 hospitals

Exclusion Criteria:

Study Design


Intervention

Other:
a cohort using Dazhuhongjingtian injection
All patients will be measured and assessed at the time Dazhuhongjingtian Injection is administered to them until they discharge. Patients using Dazhuhongjingtian Injection will be registered on a registration form including disease background, Dazhuhongjingtian Injection's administration, and extraction information from hospital information system. An adverse event or drug adverse reaction form also will be used to describe any doubted symptoms or signs from patients. A judgment will be made by doctors directly and a further analysis will be conducted by researchers to decide those potential side effects of Dazhuhongjingtian Injection.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
China Academy of Chinese Medical Sciences Hospital of Changchun University of Traditional Chinese Medicine

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of Dazhuhongjingtian's ADRs,especially number of participants with adverse events. All patients will be measured and assessed at the time Dazhuhongjingtian is administered to them until they discharge. Patients using Dazhuhongjingtian will be registered on a registration form including disease background, Dazhuhongjingtian's administration, and extraction information from hospital information system. An adverse event or drug adverse reaction form also will be used to describe any doubted symptoms or signs from patients. A judgment will be made by doctors directly and a further analysis will be conducted by researchers to decide those potential side effects of Dazhuhongjingtian. The registry procedure will last about 3 years only for patients using Dazhuhongjingtian
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