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NCT06613919

Six-months Versus Nine-months ATT for Ocular TB

Completed Phase 4 Last updated 26 September 2024
What this trial tests

Phase 4 trial testing Anti-Tuberculosis Treatment in Tuberculosis (TB) in 58 participants. Completed in 30 June 2023.

Timeline
1 January 2020
Primary endpoint
31 December 2022
30 June 2023

Quick facts

Lead sponsorL.V. Prasad Eye Institute
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment58
Start date1 January 2020
Primary completion31 December 2022
Estimated completion30 June 2023
Sites3 locations across India, Thailand, Burma

Drugs / interventions tested

Conditions studied

Sponsor

L.V. Prasad Eye Institute

Who can join

18 and older, any sex, with Tuberculosis (TB) or Uveitis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to learn if 6-months anti-TB therapy is not worse than 9-months therapy for the treatment of tubercular posterior uveitis. The main questions it aims to answer are: Does six-month therapy work as well as the nine-month therapy? Do any of the specific phenotypes of TB posterior uveitis respond better to any specific duration of anti-TB therapy? Participants: Took the standard dose of six- or nine-month ATT for TB posterior uveitis Visit the clinic as advised for checkups and tests

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Tuberculosis (TB)

Currently open trials in the same condition.

Other L.V. Prasad Eye Institute trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06613919.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing