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

> **NCT02812199** · NA · UNKNOWN · sponsor: **STS Medical** · enrollment: 30 (estimated)

## Conditions studied

- Chronic Sinusitis

## Interventions

- **DEVICE:** Composite Removable Sinus Stent
- **DRUG:** adrenaline-lidocaine
- **PROCEDURE:** cold saline wash

## Key facts

- **NCT ID:** NCT02812199
- **Lead sponsor:** STS Medical
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2016-08
- **Primary completion:** 2017-12
- **Final completion:** 2017-12
- **Target enrollment:** 30 (ESTIMATED)
- **Last updated:** 2017-05-02


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02812199

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02812199, "Efficacy of Post-FESS Implantation of Composite Removable Sinus Stent to Prevent Post-Operative Complications". Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/clinical/NCT02812199. Licensed CC0.

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