- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03091244
Surveillance for Early Liver Injuries Caused by Xianlin Gubao Capsule.
A Registry Study to Surveil Early Liver Injuries Caused by Xianlin Gubao Capsule (XLGB Capsule)
Study Overview
Status
Conditions
Detailed Description
The primary objectives of this study include:
(i) The detection of patients with serum liver biochemistry abnormalities within 8 weeks after intake of XLGB Capsule; (ii) The record of overall individuals with demographics, underlying diseases, physical status, medication information, clinical laboratory index, and so on; (iii) The specimen collection of surveiled individuals. (iv) The attempt to establish a predictive model to screen susceptibilities to XLGB Capsule.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Beijing
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Beijing Shi, Beijing, China, 100039
- 302 Military Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Individuals in accordance with indications for XLGB Capsule, including osteoarthritis, and lumbar muscle strain;
- The age range of 18 to 70 years;
- Individuals taking XLGB Capsule over 2 weeks;
Abnormalities of serum liver biochemistry achieving one of the criteria as follows:
(i) alanine aminotransaminase (ALT) or aspartate transaminase (AST) ≥2 folds of upper limit of normal (ULN); (ii) total bilirubin (TBiL) ≥ 2 ULN; (iii) alkaline phosphatase (ALP) ≥ 2 ULN;
- Individuals can provide informed consent form.
Exclusion Criteria:
- Individuals without indications for XLGB Capsule;
- Unconformity to the XLGB Capsule drug label;
- Individual taking XLGB Capsule less than 2 weeks;
- Individuals taking other hepatotoxic drugs combined with XLGB Capsule, simultaneously;
- Unconformity to the diagnostic standard for herb-induced liver injury (the Guideline for Diagnosis and Treatment of Herb-induced Liver Injury, RPGIP-2016CN003).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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The individuals taking XLGB Capsule
The overall individuals taking XLGB Capsule with recommended dosage and achieving the inclusion criteria.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The detection of patients with serum liver biochemistry abnormalities within 8 weeks after intake of XLGB Capsule.
Time Frame: participants will be followed duration intake of XLGB Capsule, an expected average within 8 weeks
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The detection of patients with serum liver biochemistry abnormalities within 8 weeks after intake of XLGB Capsule.
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participants will be followed duration intake of XLGB Capsule, an expected average within 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Clinical features of early liver injuries caused by XLGB Capsule assessed by serum parameters of liver function.
Time Frame: participants will be followed duration intake of XLGB Capsule, an expected average of 8 weeks
|
Clinical features of early liver injuries caused by XLGB Capsule assessed by serum parameters of liver function.
|
participants will be followed duration intake of XLGB Capsule, an expected average of 8 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Disease progression of early liver injuries caused by XLGB Capsule, i.e. death, liver failure, chronic DILI, recovery.
Time Frame: 8 weeks
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Disease progression of early liver injuries caused by XLGB Capsule, i.e. death, liver failure, chronic DILI, recovery.
|
8 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 302-xxh-XLGBC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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