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NCT06574529

Video-observed Therapy for Active Tuberculosis: a Feasibility Study

Completed NA Last updated 8 September 2025
What this trial tests

NA trial testing Video-observed therapy (vDOT) in Tuberculosis Active in 51 participants. Completed in 31 May 2024.

Timeline
26 November 2021
Primary endpoint
18 July 2023
31 May 2024

Quick facts

Lead sponsorLigue Pulmonaire Genevoise
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment51
Start date26 November 2021
Primary completion18 July 2023
Estimated completion31 May 2024
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

Ligue Pulmonaire Genevoise

Who can join

16 and older, any sex, with Tuberculosis Active. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Tuberculosis (TB) is still present in Switzerland, and concerns mainly foreign-born subjects. Monitoring compliance to treatment by Directly Observed Therapy (DOT) is strongly encouraged by the World Health Organization (WHO). It is however time-consuming, costly and stigmatising. This study aims to examine the feasibility of monitoring compliance through a secured web platform and videos sent via an application on a cellphone, a concept known as vDOT (Video-observed therapy). The study aims to include all patients treated for tuberculosis is on our area during an 18 month period and monitor acceptance, compliance, and technical issues related to vDOT.

Publications & conference data

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

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Other recruiting trials for Tuberculosis Active

Currently open trials in the same condition.

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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/NCT06574529.

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