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TBTC Study 28: Moxifloxacin Versus Isoniazid for TB Treatment
NCT00144417 · View on ClinicalTrials.gov ↗
Study Summary
This double-blind, randomized controlled trial evaluates moxifloxacin versus isoniazid in daily treatment during the first two months of treatment with rifampin, pyrazinamide and ethambutol for sputum smear-positive pulmonary tuberculosis.
Conditions Studied
Interventions
- DRUG Moxifloxacin (with rifampin, pyrazinamide, and ethambutol)
- DRUG isoniazid
Study Locations (20)
California
- University of Southern California Medical Center — Los Angeles
- University of California at San Diego — San Diego
- University of California, San Francincisco — San Francisco
Texas
- University of North Texas Health Science Center — Fort Worth
- Houston Veterans Administration Medical Center — Houston
- Audie L Murphy Memorial Veterans Administration Medical Center — San Antonio
Illinois
- Northwestern University — Chicago
- Hines Veterans Administration Medical Center — Hines
New York
- Columbia University — New York
- Harlem Hospital, Columbia University — New York
Arkansas
- Veterans Administration Medical Center of Arkansas — Little Rock
Colorado
- Denver Public Health Department — Denver
District of Columbia
- Washington DC Veterans Administration Medical Center — Washington D.C.
Georgia
- Emory University School of Medicine — Atlanta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 433 participants |
| Start Date | 2006-02 |
| Est. Completion | 2007-12 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00144417
The ClinicalTrials.gov registry entry for NCT00144417 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 433 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Centers for Disease Control and Prevention, which has 42 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Tuberculosis appearing as the primary indexed condition, and to 2 interventions — of which Moxifloxacin (with rifampin, pyrazinamide, and ethambutol) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00144417 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, Texas, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00144417 about?
NCT00144417 is a clinical study titled "TBTC Study 28: Moxifloxacin Versus Isoniazid for TB Treatment". This double-blind, randomized controlled trial evaluates moxifloxacin versus isoniazid in daily treatment during the first two months of treatment with rifampin, pyrazinamide and ethambutol for sputum smear-positive pulmonary tuberculosis.
What is the current status of trial NCT00144417?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 433 participants. The study started on 2006-02. Estimated completion is 2007-12.
What conditions does trial NCT00144417 study?
This clinical trial studies the following conditions: Tuberculosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00144417?
The interventions under investigation include: Moxifloxacin (with rifampin, pyrazinamide, and ethambutol) (DRUG), isoniazid (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00144417?
This trial is sponsored by Centers for Disease Control and Prevention, which has 42 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00144417 being conducted?
This trial has 20 study locations across Arkansas, California, Colorado, District of Columbia, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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