At a glance
ClinicalIndex Comparison RecordN/ACompleted· 50 enrolled
Drug / intervention
PROPEL Mini Sinus Implant +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 Propel Mini Sinus Implant Placement in the Frontal Sinus Ostia Following In-office Dilation
In Brief
A clinical study evaluating PROPEL Mini Sinus Implant and Balloon Sinus Dilation Alone for Chronic Sinusitis. Completed, enrolled 50 participants across 9 sites.
Detailed Summary
A randomized controlled trial
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Sinusitis
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
Enrollment StartAug 2016
First PostedAug 2016
Primary CompletionDec 2016
Study CompletionJun 2017
TodayJul 2026
First PostedAug 26, 2016
Enrollment StartAug 1, 2016
Primary CompletionDec 1, 2016
Study CompletionJun 1, 2017
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 9.8 years ago
Interventions
PROPEL Mini Sinus Implantdevice
Sinus implant with 370 mcg of mometasone furoate released over 30 days
Balloon Sinus Dilation Aloneprocedure