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NCT07058233

Oral Nutritional Supplementation and Weight Changes During Therapy in Malnourished Patients With Resistant Tuberculosis: A Clinical Trial

Completed NA Last updated 10 July 2025
What this trial tests

NA trial testing Oral nutritional supplementation in Tuberculosis Multi Drug Resistant Active in 70 participants. Completed in 30 December 2022.

Timeline
1 April 2022
Primary endpoint
30 December 2022
30 December 2022

Quick facts

Lead sponsorRSUP Persahabatan
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment70
Start date1 April 2022
Primary completion30 December 2022
Estimated completion30 December 2022
Sites1 location across Indonesia

Drugs / interventions tested

Conditions studied

Sponsor

RSUP Persahabatan

Who can join

Adults 15 to 65, any sex, with Tuberculosis Multi Drug Resistant Active or Rifampin-Resistant Pulmonary Tuberculosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Tuberculosis increases energy demands and protein breakdown, leading to muscle wasting. Malnutrition and minimal weight gain less than 5% in first two months predict treatment failure. Malnutrition is defined as weight loss more than 5% in three months and Body Mass Index (BMI) ≤ 20 kg/m². This study assesses weight changes with high-energy, high-protein oral nutritional supplementation (ONS).

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 trials of Oral nutritional supplementation

Trials testing the same drug.

Other RSUP Persahabatan 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/NCT07058233.

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