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NCT02027532 · ClinicalTrials.gov registry record · NA
Prevention of Infection in Closed Fractures: Cefazolin Versus Vancomycin
A NA study, sponsored by University of Tennessee.
- Terminated
- Registry status
- NA
- Development phase
- 430
- Enrollment target
NCT02027532: Clinical Trial NA study, sponsored by University of Tennessee.
NCT02027532 is a NA study that was terminated before completion, run by University of Tennessee. The registered enrollment target is 430 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02027532, a NA study, was terminated before completion, sponsored by University of Tennessee.
- TERMINATED
- Registry status
- NA
- Development phase
- 430 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the incidence rate of infection in surgical patients with closed fractures treated prophylactically with Cefazolin versus Vancomycin in the peri-operative period. The hypothesis of this study is that patients undergoing surgical treatment for closed fractures who are treated prophylactically with Vancomycin will have a lower incidence rate of infection than patients who are treated prophylactically with Cefazolin.
Interventions
- DRUG Vancomycin
- DRUG Cefazolin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 430 participants |
| Start Date | 2009-10 |
| Est. Completion | 2017-12 |
| Phase | NA |
Why NCT02027532 stopped before completion
NCT02027532 is an interventional study that assigns participants to a tested intervention. The registered 430 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 (69% lower).
The record links to 0 conditions, and to 2 interventions - of which Vancomycin is the first listed.
NCT02027532 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02027532 about?
NCT02027532 is a clinical study titled "Prevention of Infection in Closed Fractures: Cefazolin Versus Vancomycin". The purpose of this study is to compare the incidence rate of infection in surgical patients with closed fractures treated prophylactically with Cefazolin versus Vancomycin in the peri-operative period. The hypothesis of this study is that patients undergoing surgical treatment for closed fractures...
What is the current status of trial NCT02027532?
This trial is currently terminated. It is a NA study. The enrollment target is 430 participants. The study started on 2009-10. Estimated completion is 2017-12.
What interventions are being tested in trial NCT02027532?
The interventions under investigation include: Vancomycin (DRUG), Cefazolin (DRUG).
Who is sponsoring clinical trial NCT02027532?
This trial is sponsored by University of Tennessee, which has 96 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02027532's enrollment target sits among peer trials
430 235th of 2000 higher than 1,765 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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