Trials / Completed
CompletedNCT02284347
NuVent™ Revision Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 51 (actual)
- Sponsor
- Medtronic Surgical Technologies · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective, non-randomized, single-arm study designed to assess the safety and device performance of the NuVent navigation-guided balloon system for use in subjects with scarred, granulated, or previously surgically altered tissue (revision).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Electromagnetic Sinus Dilation System (NuVent™) | NuVent navigation-guided balloon system may be used to locate and move tissue, bone or cartilaginous tissue obstructing the drainage pathways of the frontal, maxillary, and sphenoid sinuses that is scarred, granulated or previously surgically-altered to facilitate dilation of the sinus ostia. |
Timeline
- Start date
- 2014-12-01
- Primary completion
- 2015-05-01
- Completion
- 2015-05-01
- First posted
- 2014-11-06
- Last updated
- 2016-08-24
- Results posted
- 2016-08-24
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02284347. Inclusion in this directory is not an endorsement.