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NCT01962961 · ClinicalTrials.gov registry record · Phase 1
N-acetylcysteine to Reduce Oxidative Stress and Improve Endothelial Function in HIV-infected Older Adults
A Phase 1 study of HIV and Endothelial Dysfunction, sponsored by Indiana University.
- Completed
- Registry status
- Phase 1
- Development phase
- 24
- Enrollment target
- 1
- Study location
NCT01962961: Completed Phase 1 study of HIV and Endothelial Dysfunction, sponsored by Indiana University.
NCT01962961 is a Phase 1 study of HIV and Endothelial Dysfunction that has completed, run by Indiana University. The registered enrollment target is 24 participants, below the 440-participant average among 303 other HIV trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01962961, a Phase 1 study of HIV and Endothelial Dysfunction, has completed, sponsored by Indiana University.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 24 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this study is to determine if n-acetylcysteine, given as PharmaNAC, reduces oxidative stress and improves vascular function in HIV-infected older adults already on HIV treatment.
Primary Outcome
Measure of oxidative stress
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT PharmaNAC (N-acetylcysteine)
- DIETARY_SUPPLEMENT Matching placebo
Study Locations (1)
Indiana
- Indiana University Health University Hospital, Indiana Clinical Research Center - Indianapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2013-10 |
| Est. Completion | 2015-10 |
| Phase | Phase 1 |
What the finished NCT01962961 record still lists
NCT01962961 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 440-participant average among 303 other HIV trials with a reported enrollment target (95% lower).
The record links to 3 conditions, with HIV appearing as the primary indexed condition, and to 2 interventions - of which PharmaNAC (N-acetylcysteine) is the first listed.
NCT01962961 reports a single indexed study location in Indiana.
Frequently Asked Questions
What is clinical trial NCT01962961 about?
NCT01962961 is a clinical study titled "N-acetylcysteine to Reduce Oxidative Stress and Improve Endothelial Function in HIV-infected Older Adults". The goal of this study is to determine if n-acetylcysteine, given as PharmaNAC, reduces oxidative stress and improves vascular function in HIV-infected older adults already on HIV treatment.
What is the current status of trial NCT01962961?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2013-10. Estimated completion is 2015-10.
What conditions does trial NCT01962961 study?
This clinical trial studies the following conditions: HIV, Endothelial Dysfunction, Oxidative Stress.
What interventions are being tested in trial NCT01962961?
The interventions under investigation include: PharmaNAC (N-acetylcysteine) (DIETARY_SUPPLEMENT), Matching placebo (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT01962961?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01962961 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Where NCT01962961's enrollment target sits among peer trials
24 279th of 303 higher than 23 of 303 other HIV trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other HIV 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.
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