Trials / Completed
CompletedNCT01714687
Comparison of Balloon Sinuplasty In-Office Versus Medical Management for Recurrent Acute Sinusitis Patients (CABERNET)
Comparison of Balloon Sinuplasty In-Office Versus Medical Management for Recurrent Acute Sinusitis Patients: A Randomized Controlled Study (CABERNET)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 59 (actual)
- Sponsor
- Integra LifeSciences Corporation · Industry
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | balloon sinus dilation | |
| OTHER | medical therapy |
Timeline
- Start date
- 2012-10-01
- Primary completion
- 2015-10-01
- Completion
- 2016-04-01
- First posted
- 2012-10-26
- Last updated
- 2024-07-12
- Results posted
- 2019-03-11
Locations
5 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT01714687. Inclusion in this directory is not an endorsement.