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NCT00939393 · ClinicalTrials.gov registry record · NA
Balloon Sinus Dilation In Office or OR
A NA study, sponsored by Integra LifeSciences Corporation.
- Completed
- Registry status
- NA
- Development phase
- 72
- Enrollment target
NCT00939393 is a NA study that has completed, run by Integra LifeSciences Corporation. The registered enrollment target is 72 participants.
The verdict
NCT00939393, a NA study, has completed, sponsored by Integra LifeSciences Corporation.
- COMPLETED
- Registry status
- NA
- Development phase
- 72 participants
- Enrollment target
Study Summary
Endoscopic sinus surgery will be performed either in the physician's office or in the operating room (OR). Patients treated in the physician's office will have endoscopic sinus surgery performed with balloon sinuplasty devices. Patients treated in the OR will have endoscopic sinus surgery performed with or without balloon sinuplasty devices.
Interventions
- DEVICE FESS instruments with or without balloon treatment
- DEVICE Balloon Sinuplasty
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2008-04-01 |
| Est. Completion | 2010-07-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00939393
The ClinicalTrials.gov registry entry for NCT00939393 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Integra LifeSciences Corporation, which has 60 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which FESS instruments with or without balloon treatment is the first listed.
NCT00939393 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00939393 about?
NCT00939393 is a clinical study titled "Balloon Sinus Dilation In Office or OR". Endoscopic sinus surgery will be performed either in the physician's office or in the operating room (OR). Patients treated in the physician's office will have endoscopic sinus surgery performed with balloon sinuplasty devices. Patients treated in the OR will have endoscopic sinus surgery performed ...
What is the current status of trial NCT00939393?
This trial is currently completed. It is a NA study. The enrollment target is 72 participants. The study started on 2008-04-01. Estimated completion is 2010-07-01.
What interventions are being tested in trial NCT00939393?
The interventions under investigation include: FESS instruments with or without balloon treatment (DEVICE), Balloon Sinuplasty (DEVICE).
Who is sponsoring clinical trial NCT00939393?
This trial is sponsored by Integra LifeSciences Corporation, which has 60 total clinical trials registered on ClinicalTrials.gov.
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