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Lead
SinuSys Corporation
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
Age
18–75
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Diagnosis of chronic maxillary sinusitis
You may not be if
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
