At a glance
ClinicalIndex Comparison RecordN/ACompleted· 82 enrolled
Drug / intervention
XprESS Multi-Sinus Dilation Tooldevice
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.
Trans-Nasal Maxillary Multi-Sinus Balloon Dilation Study
In Brief
A clinical study evaluating XprESS Multi-Sinus Dilation Tool for Sinusitis. Completed, enrolled 82 participants across 1 site.
Detailed Summary
The purpose of this study is to show clinically meaningful improvement in symptom severity after transnasal balloon dilation of the maxillary sinus outflow tract with or without balloon dilation of the frontal or sphenoid sinuses.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSinusitis
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartApr 2012
First PostedJun 2012
Primary CompletionOct 2013
TodayJul 2026
First PostedJun 6, 2012
Enrollment StartApr 1, 2012
Primary CompletionOct 1, 2013
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 14.1 years ago
Interventions
XprESS Multi-Sinus Dilation Tooldevice
Sinus balloon dilation