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Trial registered on ANZCTR
Registration number
ACTRN12610000643077
Ethics application status
Approved
Date submitted
4/08/2010
Date registered
9/08/2010
Date last updated
8/04/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
Effect of silymarin in treatment of adverse effects of anti tuberculosis drugs.
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Scientific title
Evaluation of Silymarin in treatment of anti tuberculosis drug induced hepatitis in patients newly diagnosed with tuberculosis.
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Secondary ID [1]
252357
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Nill
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Tuberculosis
257866
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Condition category
Condition code
Infection
258030
258030
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0
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Other infectious diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Silymarin 420 mg per day,in three doses, It will start after diagnosis of drug induced hepatitis and stop after normalization of liver function tests, as oral tablets
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Intervention code [1]
256934
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Treatment: Drugs
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Comparator / control treatment
Lactose 420 mg per day,in three doses, It will start after diagnosis of drug induced hepatitis and stop after normalization of liver function tests, as oral tablets
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Normalization of liver function tests
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Assessment method [1]
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Timepoint [1]
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Evaluation of liver function tests three times weekly from diagnosis of drug induced hepatitis (Drug induced hepatitis means 3 times elevation of liver enzymes with clinical symptoms or 5 times without symptoms.)until normalization of them.
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Secondary outcome [1]
265051
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Incidence of silymarin adverse effects i. e. nausea, vomiting, bloating, diarrhea, itching by patient questionnaires and daily checklist.
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Assessment method [1]
265051
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Timepoint [1]
265051
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Continuously during administration of drug/placebo
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Eligibility
Key inclusion criteria
New cases of tuberculosis
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Minimum age
18
Years
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Maximum age
100
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. Infection with Human Immune deficiency virus 2. Infection with hepatitis B virus 3. Infection with hepatitis c virus 4.pregnancy 5. Breast feeding
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/10/2010
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
60
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
2757
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Iran, Islamic Republic Of
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State/province [1]
2757
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Tehran
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Funding & Sponsors
Funding source category [1]
257383
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University
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Name [1]
257383
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Shahid Beheshti medical university
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Address [1]
257383
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Velenjak street, Evin, Tehran, post code: 1955841452
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Country [1]
257383
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Iran, Islamic Republic Of
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Funding source category [2]
257384
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University
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Name [2]
257384
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Shahid Beheshti medical university
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Address [2]
257384
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Velenjak street, Evin, Tehran, post code: 1955841452
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Country [2]
257384
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Iran, Islamic Republic Of
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Funding source category [3]
257385
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University
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Name [3]
257385
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Shahid Beheshti medical university
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Address [3]
257385
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Velenjak street, Evin, Tehran, post code: 1955841452
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Country [3]
257385
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Iran, Islamic Republic Of
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Primary sponsor type
Government body
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Name
National Institute of Tuberculosis and Lung Disease (NRITLD)
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Address
Dar Abad street, Niavaran, Tehran, post code: 1955841452
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Country
Iran, Islamic Republic Of
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Secondary sponsor category [1]
256623
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Hospital
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Name [1]
256623
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Masih Daneshvari Hospital
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Address [1]
256623
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Dar Abad street, Niavaran, Tehran, post code: 1955841452
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Country [1]
256623
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Iran, Islamic Republic Of
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
Adverse effects of antituberculosis drugs are frequent, sometimes with morbidity and even may be fatal, most serious of them is drug induced hepatitis. As Sylimarin in rat model has been effective in prevention and treatment of hepatic adverse effects of anti tuberculosis drugs, we decide to investigate this study.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Majid Marjani
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Address
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Masih Daneshvari Hospital, Dar Abad, Niavaran, Tehran
Post code: 1956944413
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Country
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Iran, Islamic Republic Of
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Phone
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+982126109590
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Fax
31384
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Email
31384
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[email protected]
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Contact person for public queries
Name
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Majid Marjani
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Address
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National Institute of Tuberculosis and Lung Disease, Masih Daneshvari Hospital, Dar Abad street, Niavaran, Tehran, post code:1955841452
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Country
14631
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Iran, Islamic Republic Of
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Phone
14631
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+982126109590
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Fax
14631
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Email
14631
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[email protected]
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Contact person for scientific queries
Name
5559
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Majid Majani
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Address
5559
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National Institute of Tuberculosis and Lung Disease, Masih Daneshvari Hospital, Dar Abad street, Niavaran, Tehran, post code:1955841452
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Country
5559
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Iran, Islamic Republic Of
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Phone
5559
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+982126109590
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Fax
5559
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Email
5559
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Evaluation of Silymarin for management of anti-tuberculosis drug induced liver injury: A randomized clinical trial.
2019
https://dx.doi.org/10.22037/ghfbb.v12i2.1562
N.B. These documents automatically identified may not have been verified by the study sponsor.
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