drugset / Trial / NCT02812199
Efficacy of Post-FESS Implantation of Composite Removable Sinus Stent to Prevent Post-Operative Complications
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Background | Epinephrine | Other / unclassified | — | Other |
| Background | Lidocaine | Other / unclassified | — | Other |