Clinical Trials Directory

Trials / Completed

CompletedNCT01554280

Fully Coated, Removable, Self-expanding Oesophageal Stents for Preventing Strictures Following Complete Barretts Excision.

Fully, Coated, Removable, Self-expanding Oesophageal Stents for the Prevention of Oesophageal Stricture Following Endoscopic Mucosal Resection of Short Segment Barrett's With High Grade Dysplasia and Early Cancer.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Professor Michael Bourke · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate whether preventative placement of a removable oesophageal stent reduces the rate of scar tissue, or stricture formation after removing the precancerous or early cancerous Barrett's mucosa by Endoscopic Mucosal Resection (EMR). The stent will be placed 10-14 days after initial EMR. The stent will then be removed 8 weeks later by repeat Endoscopy. Patients will be followed up weekly following insertion of the oesophageal stent.

Conditions

Interventions

TypeNameDescription
DEVICEFully coated, removable , self-expanding oesophageal stentInsertion of the fully coated, removable, self-expanding oesophageal stent for the prevention of oesophageal strictures.

Timeline

Start date
2012-01-01
Primary completion
2013-01-01
Completion
2014-01-01
First posted
2012-03-14
Last updated
2021-03-23

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT01554280. Inclusion in this directory is not an endorsement.