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Surveillance for Early Liver Injuries Caused by Yangxue Shengfa Capsule.

B

Beijing 302 Hospital

Status

Unknown

Conditions

Drug-Induced Liver Injury

Study type

Observational

Funder types

Other

Identifiers

NCT03113838
302-xxh-YXSFC

Details and patient eligibility

About

This is a prospective registry study to surveil early liver injuries caused by Yangxue Shengfa Capsule (YXSF Capsule) through a non-intervention observational way. And attempt to establish a predictive model to screen susceptibilities to YXSF Capsule.

Full description

The primary objectives of this study include:

(i) The detection of patients with serum liver biochemistry abnormalities less than 8 weeks after intake of YXSF 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 YXSF Capsule.

Enrollment

1,000 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Individuals in accordance with indications for YXSF Capsule, including xerasia, itchy scalp, alopecia areata, seborrheic dermatitis and alopecia;

  2. The age range of 18 to 70 years;

  3. Individuals taking YXSF Capsule over 2 weeks;

  4. 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;

  5. Individuals can provide informed consent form.

Exclusion criteria

  1. Individuals without indications for YXSF Capsule;
  2. Inconformity to the YXSF Capsule drug label;
  3. Individual taking YXSF Capsule less than 2 weeks;
  4. Individuals taking other hepatotoxic drugs combined with YXSF Capsule, simultaneously;
  5. Inconformity to the diagnostic standard for herb-induced liver injury (the Guideline for Diagnosis and Treatment of Herb-induced Liver Injury, RPGIP-2016CN003).

Trial design

1,000 participants in 1 patient group

Taking YXSF Capsule Group
Description:
The overall individuals taking YXSF Capsule and achieving the inclusion criteria.

Trial contacts and locations

1

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Central trial contact

Jia-bo Wang; Xiao-he Xiao

Data sourced from clinicaltrials.gov

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