At a glance
ClinicalIndex Comparison RecordN/ACompleted· 50 enrolled
Drug / intervention
non-coated Intranasal Splint +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Clinical Evaluation of the Steroid-Eluting Sinexus Intranasal Splint Used Following Functional Endoscopic Sinus Surgery (FESS) in Patients With Chronic Rhinosinusitis (CRS)
In Brief
A clinical study evaluating non-coated Intranasal Splint and Sinexus Intranasal Splint for Chronic Sinusitis. Completed, enrolled 50 participants across 1 site.
Detailed Summary
The purpose of this study is to assess the safety and performance of the Sinexus Intranasal Splint when used following Functional Endoscopic Sinus Surgery (FESS) in patients with Chronic Rhinosinusitis.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Sinusitis
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartMar 2008
First PostedFeb 2009
Primary CompletionMar 2009
Study CompletionApr 2009
TodayJul 2026
First PostedFeb 11, 2009
Enrollment StartMar 1, 2008
Primary CompletionMar 1, 2009
Study CompletionApr 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 17.4 years ago
Interventions
non-coated Intranasal Splintdevice
placement of non-coated intranasal splint following FESS
Sinexus Intranasal Splintdevice
placement of Sinexus Intranasal Splint placed following FESS