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NCT05306704: HDVDS-HIVT

High-Dose Vitamin D3 Supplementation in the Treatment of Human Immune Deficiency Virus Patients Trial

Completed Phase 3 Last updated 11 April 2022
What this trial tests

Phase 3 trial testing placebo Oil in HIV-1-infection in 95 participants. Completed in 31 January 2022.

Timeline
15 February 2019
Primary endpoint
31 January 2022
31 January 2022

Quick facts

Lead sponsorUniversity of the Punjab
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposesupportive care
Enrollment95
Start date15 February 2019
Primary completion31 January 2022
Estimated completion31 January 2022
Sites2 locations across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

University of the Punjab

Who can join

19 and older, any sex, with HIV-1-infection or Hypovitaminosis D. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

High-Dose Vitamin D3 in the Treatment of Human Immune Deficiency Virus Patients, A Double-Blind Randomized Control Trial Human immunodeficiency virus is a key challenge for global health. Vitamin D deficiency is common in people living with HIV infection. Antiretroviral therapy may create unique risk factors for vitamin D insufficiency, including alterations of vitamin D metabolism by ART.

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 25-Hydroxyvitamin D

Trials testing the same drug.

Other recruiting trials for HIV-1-infection

Currently open trials in the same condition.

Other University of the Punjab 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/NCT05306704.

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