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The Efficacy of Silymarin on the Prevention of Hepatotoxicity From Antituberculosis Drugs

Primary Purpose

Tuberculosis

Status
Completed
Phase
Not Applicable
Locations
Thailand
Study Type
Interventional
Intervention
silymarin
Placebo
Sponsored by
Ramathibodi Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Tuberculosis focused on measuring Drug-induced liver injury, Tuberculosis, Silymarin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • tuberculosis cases
  • treated with isoniazid, rifampicin, ethambutol and pyrazinamide

Exclusion Criteria:

  • no known liver disease (HBV, HCV), and HIV infection
  • normal ALT level before enrollment
  • refuse to participate

Sites / Locations

  • Gastroenterology and Hepatology, Ramathibodi hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

silymarin

placebo

Arm Description

Silymarin 140 mg three times a day for 4 weeks

Placeo 1 tab three times a day for 4 weeks

Outcomes

Primary Outcome Measures

The number of patients who develop drug-induced liver injury (DILI) at 4 weeks
DILI from anti-tuberculosis drugs ('atb-DILI') is defined as: i) a rise of alanine aminotransferase (ALT) to 2 times above normal upper limit, or ii) an elevation of total bilirubin more than 2 mg/dl with or without ALT elevation.

Secondary Outcome Measures

Full Information

First Posted
February 21, 2013
Last Updated
December 23, 2013
Sponsor
Ramathibodi Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01800487
Brief Title
The Efficacy of Silymarin on the Prevention of Hepatotoxicity From Antituberculosis Drugs
Official Title
The Efficacy of Silymarin on the Prevention of Hepatotoxicity From Antituberculosis Drugs
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ramathibodi Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hepatitis is one of the most common adverse effect from anti-tuberculosis. Silymarin showed its efficacy to decreased serum alanine transaminase enzyme in animal models from recent study. No confirmed this efficacy was performed in human. A prospective, double-blind, placebo-controlled trial was carried out according to Good Clinical Practice Guideline. This study is to define the efficacy of silymarin to prevent hepatotoxicity from anti-tuberculosis drugs. Informed consent is obtained prior to the study. New patients diagnosed with tuberculosis are enrolled. Patients with liver diseases, current alcohol drinking more than 20 g/day, regular use of herbal or other potential hepatotoxic drugs are excluded. Patients are treated with a standard regimen of four anti-tuberculosis therapy. They will randomize to receive either placebo or silymarin (140 mg) thrice daily. Liver function test (LFT) and clinical changes are assessed at 2- and 4-week after initiation of the treatment. DILI from anti-tuberculosis drugs ('atb-DILI') is defined as: i) a rise of alanine aminotransferase (ALT) to 2 times above normal upper limit, or ii) an elevation of total bilirubin more than 2 mg/dl with or without ALT elevation. The study endpoints are the level of ALT by week 4 and the number of patients who developed atb-DILI. Statistical analysis is used to compare the differences in ALT and number of atb-DILI
Detailed Description
- Prevention of antituberculosis-related drug induced liver injury with silymarin is investigated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
Drug-induced liver injury, Tuberculosis, Silymarin

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
silymarin
Arm Type
Active Comparator
Arm Description
Silymarin 140 mg three times a day for 4 weeks
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
Placeo 1 tab three times a day for 4 weeks
Intervention Type
Drug
Intervention Name(s)
silymarin
Intervention Description
140 mg three times a day for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo (silymarin) 1 tab three times a day for 4 weeks
Primary Outcome Measure Information:
Title
The number of patients who develop drug-induced liver injury (DILI) at 4 weeks
Description
DILI from anti-tuberculosis drugs ('atb-DILI') is defined as: i) a rise of alanine aminotransferase (ALT) to 2 times above normal upper limit, or ii) an elevation of total bilirubin more than 2 mg/dl with or without ALT elevation.
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: tuberculosis cases treated with isoniazid, rifampicin, ethambutol and pyrazinamide Exclusion Criteria: no known liver disease (HBV, HCV), and HIV infection normal ALT level before enrollment refuse to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abhasnee Sobhonslidsuk, MD
Organizational Affiliation
Ramathibodi Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Chote Luangchosiri, MD
Organizational Affiliation
Ramathibodi
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gastroenterology and Hepatology, Ramathibodi hospital
City
Bangkok
ZIP/Postal Code
10400
Country
Thailand

12. IPD Sharing Statement

Citations:
PubMed Identifier
26400476
Citation
Luangchosiri C, Thakkinstian A, Chitphuk S, Stitchantrakul W, Petraksa S, Sobhonslidsuk A. A double-blinded randomized controlled trial of silymarin for the prevention of antituberculosis drug-induced liver injury. BMC Complement Altern Med. 2015 Sep 23;15:334. doi: 10.1186/s12906-015-0861-7.
Results Reference
derived

Learn more about this trial

The Efficacy of Silymarin on the Prevention of Hepatotoxicity From Antituberculosis Drugs

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