NCT03189927

BD-Covered Stent for Benign Esophageal Strictures: a Safety and Feasibility Study

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 15 (estimated)
• Sponsor: Radboud University Medical Center · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

A non-randomized prospective clinical, pilot study in a single centre assessing the safety and feasibility of the esophageal biodegradable covered stent for refractory benign esophageal strictures with or without fistulae

Detailed description

A non-randomized prospective clinical, pilot study in a single centre assessing the safety and feasibility of the esophageal biodegradable covered stent for refractory benign esophageal strictures with or without fistulae. The follow-up will be 6 months form implantation. After 3 months a control endoscopy will take place to evaluate stent and degradation process.

Conditions

• Benign Esophageal Stricture

Interventions

Type	Name	Description
DEVICE	BD-Covered esophageal stent	a biodegradable covered stent is implanted to achieve a long-term relieve of dysphagia in refractory benign esophageal strictures

Timeline

• Start date: 2017-07-01
• Primary completion: 2018-07-01
• Completion: 2019-01-01
• First posted: 2017-06-16
• Last updated: 2017-06-16