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COMPLETED NA

Comparison of Balloon Sinuplasty In-Office Versus Medical Management for Recurrent Acute Sinusitis Patients (CABERNET)

NCT01714687 · View on ClinicalTrials.gov ↗

Study Summary

This post-market study aims to compare health outcomes for Recurrent Acute Rhinosinusitis (RARS) patients treated with balloon sinus dilation (BSD) versus medical management alone.

Interventions

  • DEVICE balloon sinus dilation
  • OTHER medical therapy

Study Locations (5)

Texas

  • — Dallas
  • — McKinney

Alabama

  • — Birmingham

Georgia

  • — Atlanta

Nevada

  • — Las Vegas

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2012-10-01
Est. Completion 2016-04-01
Phase NA

Sponsor

Integra LifeSciences Corporation

14 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01714687

The ClinicalTrials.gov registry entry for NCT01714687 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 59 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Integra LifeSciences Corporation, which has 14 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 Recurrent Acute Rhinosinusitis appearing as the primary indexed condition, and to 2 interventions — of which balloon sinus dilation 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: NCT01714687 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Texas, Alabama, Georgia. 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 NCT01714687 about?

NCT01714687 is a clinical study titled "Comparison of Balloon Sinuplasty In-Office Versus Medical Management for Recurrent Acute Sinusitis Patients (CABERNET)". This post-market study aims to compare health outcomes for Recurrent Acute Rhinosinusitis (RARS) patients treated with balloon sinus dilation (BSD) versus medical management alone.

What is the current status of trial NCT01714687?

This trial is currently completed. It is a NA study. The enrollment target is 59 participants. The study started on 2012-10-01. Estimated completion is 2016-04-01.

What conditions does trial NCT01714687 study?

This clinical trial studies the following conditions: Recurrent Acute Rhinosinusitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01714687?

The interventions under investigation include: balloon sinus dilation (DEVICE), medical therapy (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01714687?

This trial is sponsored by Integra LifeSciences Corporation, which has 14 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01714687 being conducted?

This trial has 5 study locations across Alabama, Georgia, Nevada, 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