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Safety and Performance of the SinuSys Dilation System for Dilation of the Maxillary Sinus Ostium

Phase 1
Completed
Conditions
Sinusitis
Interventions
Device: SinuSys Dilation System
Registration Number
NCT01623050
Lead Sponsor
SinuSys Corporation
Brief Summary

The purpose of this study is to assess safety and performance of the SinuSys Dilation System for dilation of the maxillary sinus ostium.

Detailed Description

A multicenter, single-arm, prospective study conducted to assess the safety and effectiveness of a new osmotically-driven, low-pressure expansion device for dilation of maxillary sinus ostia in patients with (CRS) Chronic Rhinosinusitis

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria

-Diagnosis of chronic maxillary sinusitis

Exclusion Criteria
  • Previous antrostomy
  • Sinonasal tumours
  • Cystic fibrosis
  • History of facial trauma that distorts sinus anatomy and precludes access to the maxillary sinus
  • Pregnant or breastfeeding females
  • Currently participating in another drug or device study

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
SinuSys Dilation SystemSinuSys Dilation SystemMaxillary Sinus Dilation
Primary Outcome Measures
NameTimeMethod
Patency of Treated AreaImmediately post procedure
Secondary Outcome Measures
NameTimeMethod
Patency of Treated Area12 months

Maxillary Sinus Ostia of 27 patients analyzed.

Number of Participants With Device-related Adverse Events as a Measure of Safety3 months

Trial Locations

Locations (5)

St. Elizabeth Medical Center

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Boston, Massachusetts, United States

Palo Alto Medical Foundation

πŸ‡ΊπŸ‡Έ

Palo Alto, California, United States

Valley ENT

πŸ‡ΊπŸ‡Έ

Tucson, Arizona, United States

St. Paul's Hospital, ENT Department

πŸ‡¨πŸ‡¦

Vancouver, British Columbia, Canada

Charing Cross Hospital

πŸ‡¬πŸ‡§

London, United Kingdom

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