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COMPLETED NA

Air Barrier System Device to Reduce Contamination in Posterior Spine Surgery

NCT01559506 · View on ClinicalTrials.gov ↗

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

Conditions Studied

Interventions

  • DEVICE Air Barrier System device

Study Locations (1)

Texas

  • Michael E. DeBakey VA Medical Center — Houston

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2011-11
Est. Completion 2015-02
Phase NA

Sponsor

Nimbic Systems

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01559506

The ClinicalTrials.gov registry entry for NCT01559506 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Nimbic Systems, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01559506 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01559506?

The interventions under investigation include: Air Barrier System device (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01559506?

This trial is sponsored by Nimbic Systems, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial