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NCT01751646 · ClinicalTrials.gov registry record · NA

Vitamin D Absorption in HIV Infected Young Adults Being Treated With Tenofovir Containing cART

A NA study, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
NA
Development phase
214
Enrollment target

NCT01751646: Completed NA study, sponsored by University of North Carolina, Chapel Hill.

NCT01751646 is a NA study that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 214 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01751646, a NA study, has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
NA
Development phase
214 participants
Enrollment target

Study Summary

This is a 48 week randomized double-blind, placebo-controlled prospective cohort study of adolescents and young adults with HIV infection in the Adolescent Medicine Trials Network for HIV/AIDS Interventions (ATN) who are currently being treated with cART that includes tenofovir disoproxil fumarate (TDF) as one component of the regimen that includes at least three Food and Drug Administration (FDA)-approved antiretroviral (ARV) drugs for at least 180 days.

Primary Outcome

Percent change from baseline to week (wk) 48 in DXA-measured BMD at the spine for the randomized study groups. Lumbar spine BMD (L1 - L4) (g/cm2) change from Baseline to wk 48 visit.

Interventions

  • DIETARY_SUPPLEMENT Vitamin D3 placebo
  • DIETARY_SUPPLEMENT Vitamin D3 50,000 IU

Trial Details

FieldValue
Enrollment Target 214 participants
Start Date 2012-10
Est. Completion 2016-06
Phase NA

What the finished NCT01751646 record still lists

NCT01751646 is an interventional study that assigns participants to a tested intervention. The registered 214 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 2 interventions - of which Vitamin D3 placebo is the first listed.

NCT01751646 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01751646 about?

NCT01751646 is a clinical study titled "Vitamin D Absorption in HIV Infected Young Adults Being Treated With Tenofovir Containing cART". This is a 48 week randomized double-blind, placebo-controlled prospective cohort study of adolescents and young adults with HIV infection in the Adolescent Medicine Trials Network for HIV/AIDS Interventions (ATN) who are currently being treated with cART that includes tenofovir disoproxil fumarate (...

What is the current status of trial NCT01751646?

This trial is currently completed. It is a NA study. The enrollment target is 214 participants. The study started on 2012-10. Estimated completion is 2016-06.

What interventions are being tested in trial NCT01751646?

The interventions under investigation include: Vitamin D3 placebo (DIETARY_SUPPLEMENT), Vitamin D3 50,000 IU (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT01751646?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01751646's enrollment target sits among peer trials

214 487th of 2000 higher than 1,513 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

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Source: ClinicalTrials.gov NCT01751646, the US trial registry maintained by the National Library of Medicine. NCT01751646 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.