Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00023374 · ClinicalTrials.gov registry record · NA

TBTC Study 24: Intermittent Treatment of TB With Isoniazid Resistance or Intolerance

A NA study of Tuberculosis, sponsored by Centers for Disease Control and Prevention.

Completed
Registry status
NA
Development phase
98
Enrollment target
20
Study locations

NCT00023374: Completed NA study of Tuberculosis, sponsored by Centers for Disease Control and Prevention.

NCT00023374 is a NA study of Tuberculosis that has completed, run by Centers for Disease Control and Prevention. The registered enrollment target is 98 participants, below the 931-participant average among 29 other Tuberculosis trials with a reported enrollment target (89% lower). The trial reports 20 study locations across 13 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00023374, a NA study of Tuberculosis, has completed, sponsored by Centers for Disease Control and Prevention.

COMPLETED
Registry status
NA
Development phase
98 participants
Enrollment target
20
Study locations

Study Summary

This study is a prospective, open-label, nonrandomized trial using a largely-intermittent, six-month tuberculosis treatment regimen among patients who will not receive isoniazid due to the presence of initial isoniazid resistance or intolerance. Subjects are enrolled after resistance or intolerance to isoniazid has been documented, and are treated for a total of six months (nine months if baseline chest x-ray shows cavitation and 2-month sputum culture is positive) with twice weekly or thrice weekly rifampin, ethambutol, and pyrazinamide.

Conditions Studied

Interventions

  • DRUG Ethambutol
  • DRUG Rifampin
  • DRUG Pyrazinamide
  • DRUG REZ

Study Locations (20)

New York

  • New York University School of Medicine - New York
  • Columbia University/Presbyterian Medical Center - New York
  • Harlem Hospital Center - New York

Texas

  • University of North Texas Health Science Center - Fort Worth
  • Thomas Street Clinic - Houston
  • Audi L. Murphy VA Hospital - San Antonio

California

  • LA County/USC Medical Center - Los Angeles
  • University of California, San Francisco - San Francisco

Illinois

  • Chicago VA Medical Center (Lakeside) - Chicago
  • Hines VA Medical Center - Hines

North Carolina

  • Carolinas Medical Center - Charlotte
  • Duke University Medical Center - Durham

Arkansas

  • Central Arkansas Veterans Health System - Little Rock

Colorado

  • Denver Department of Public Health and Hospitals - Denver

District of Columbia

  • Washington, D.C. VAMC - Washington D.C.

Trial Details

FieldValue
Enrollment Target 98 participants
Start Date 2000-08
Est. Completion 2010-12
Phase NA

What the finished NCT00023374 record still lists

NCT00023374 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 98 participants, a relatively small participant target, below the 931-participant average among 29 other Tuberculosis trials with a reported enrollment target (89% lower).

The record links to 1 condition, with Tuberculosis appearing as the primary indexed condition, and to 4 interventions - of which Ethambutol is the first listed.

NCT00023374 names 20 study sites across 13 states, led by New York, Texas, California.

Frequently Asked Questions

What is clinical trial NCT00023374 about?

NCT00023374 is a clinical study titled "TBTC Study 24: Intermittent Treatment of TB With Isoniazid Resistance or Intolerance". This study is a prospective, open-label, nonrandomized trial using a largely-intermittent, six-month tuberculosis treatment regimen among patients who will not receive isoniazid due to the presence of initial isoniazid resistance or intolerance. Subjects are enrolled after resistance or intolerance ...

What is the current status of trial NCT00023374?

This trial is currently completed. It is a NA study. The enrollment target is 98 participants. The study started on 2000-08. Estimated completion is 2010-12.

What conditions does trial NCT00023374 study?

This clinical trial studies the following conditions: Tuberculosis.

What interventions are being tested in trial NCT00023374?

The interventions under investigation include: Ethambutol (DRUG), Rifampin (DRUG), Pyrazinamide (DRUG), REZ (DRUG).

Who is sponsoring clinical trial NCT00023374?

This trial is sponsored by Centers for Disease Control and Prevention, which has 139 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00023374 being conducted?

This trial has 20 study locations across Arkansas, California, Colorado, District of Columbia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Tuberculosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00023374's enrollment target sits among peer trials

98 17th of 29 higher than 13 of 29 other Tuberculosis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Tuberculosis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02926729 · 98 participants · NA

    Real-Time Assessment Of Breast Cancer Lumpectomy Specimen Margins With Nonlinear Microscopy

  • NCT03382977 · 98 participants · Phase 1

    Study to Evaluate Safety, Tolerability, and Optimal Dose of Candidate GBM Vaccine VBI-1901 in Recurrent GBM Subjects

  • NCT04577014 · 98 participants · Phase 1

    Retifanlimab (Anti-PD-1 Antibody) With Gemcitabine and Docetaxel in Patients With Advanced Soft Tissue Sarcoma

  • NCT04817618 · 98 participants · Phase 3

    Study of Efficacy and Safety of Iptacopan in Patients With C3 Glomerulopathy.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00023374, the US trial registry maintained by the National Library of Medicine. NCT00023374 (small enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.