drugset / Trial / NCT02812199

Efficacy of Post-FESS Implantation of Composite Removable Sinus Stent to Prevent Post-Operative Complications

NCT02812199 ↗

Unknown 30 enrolled STS Medical
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a randomized controlled first in man study. Study purpose is to assess safety and efficacy of Composite Removable Stent Composite Stent implantation post-endoscopic sinus surgery in terms of: * Sinus tissue adhesions * Middle turbinate lateralization into nasal septum i.e. postoperative opening reduction * Inflammation

Timeline

Start
2016-08
Primary completion
2017-12
Completion
2017-12

Drugs

EvaluationDrugModalityDoseRoute
Background Epinephrine Other / unclassified — Other
Background Lidocaine Other / unclassified — Other