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The Incidence and Risk Factors of Side Effects During the Initial Phase of Rifater Therapy - a Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01182259
Enrollment
200
Registered
2010-08-16
Start date
2009-10-31
Completion date
Unknown
Last updated
2010-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tuberculosis

Brief summary

Tuberculosis remains one of the largest health problems in the world today. Multidrug therapy is necessary to cure tuberculosis patients and to prevent the selection of drug-resistant mutants, however, which may increase the incidence of side effects during the course of treatment. These side effects may be mild as well as fatal. A severe side effect against one of the anti-TB drugs, which influences drug compliance, may lead to the discontinuation of that drug. At the same time, the risk of treatment failure and relapse are higher. Therefore monitoring the rate of anti-TB drugs induced adverse effects and the related risk factors is crucial. Awareness of the risk groups may decrease the incidence of serious drug-related side effects and medical cost. The fixed-dose combinations (FDCs) of tablets against tuberculosis is now being recommended by WHO, which simplify the prescription of drugs and prevent the development of drug resistance. However, the FDC regimen is not consistent with the dosages that are usually given, the higher risk of drug toxicity and adverse reactions should be considered. To our knowledge, there was no report to assess the adverse effects of FDC anti-TB drugs in Taiwan. The aim of the present study is to investigate the current incidence of side effects and the risk factors related to FDC drugs for side effects during the initial phase of therapy.

Interventions

None listed

Sponsors

E-DA Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Newly diagnosed pulmonary TB and extrapulmonary TB patients 2. No previous anti-TB drugs treatment 3. Age more than 18years old

Exclusion criteria

1. Expected life \< 6months 2. Baseline AST and ALT \> 3 fold upper limit of normal (ULN) or total bilirubin\>2mg/dl 3. Age less than 18years old

Countries

Taiwan

Contacts

Primary ContactJiun-Ting Wu, MD
ed103621@edah.org.tw886-7-615-0011

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026