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NCT01559506 · ClinicalTrials.gov registry record · NA
Air Barrier System Device to Reduce Contamination in Posterior Spine Surgery
A NA study of Surgery, sponsored by Nimbic Systems.
- Completed
- Registry status
- NA
- Development phase
- 41
- Enrollment target
- 1
- Study location
NCT01559506: Completed NA study of Surgery, sponsored by Nimbic Systems.
NCT01559506 is a NA study of Surgery that has completed, run by Nimbic Systems. The registered enrollment target is 41 participants, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01559506, a NA study of Surgery, has completed, sponsored by Nimbic Systems.
- COMPLETED
- Registry status
- NA
- Development phase
- 41 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this study is to determine whether the Air Barrier System (ABS) reduces airborne colony-forming units (e.g. bacteria) present at surgery sites during posterior spinal procedures
Primary Outcome
Colony-forming unit density at incision site (CFU/m3)
Conditions Studied
Interventions
- DEVICE Air Barrier System device
Study Locations (1)
Texas
- Michael E. DeBakey VA Medical Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 41 participants |
| Start Date | 2011-11 |
| Est. Completion | 2015-02 |
| Phase | NA |
What the finished NCT01559506 record still lists
NCT01559506 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower).
The record links to 1 condition, with Surgery appearing as the primary indexed condition, and to 1 intervention - of which Air Barrier System device is the first listed.
NCT01559506 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT01559506 about?
NCT01559506 is a clinical study titled "Air Barrier System Device to Reduce Contamination in Posterior Spine Surgery". The objective of this study is to determine whether the Air Barrier System (ABS) reduces airborne colony-forming units (e.g. bacteria) present at surgery sites during posterior spinal procedures
What is the current status of trial NCT01559506?
This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2011-11. Estimated completion is 2015-02.
What conditions does trial NCT01559506 study?
This clinical trial studies the following conditions: Surgery.
What interventions are being tested in trial NCT01559506?
The interventions under investigation include: Air Barrier System device (DEVICE).
Who is sponsoring clinical trial NCT01559506?
This trial is sponsored by Nimbic Systems, which has 4 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01559506 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01559506's enrollment target sits among peer trials
41 99th of 120 higher than 22 of 120 other Surgery trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Surgery 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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