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
| Type | Name | Description |
|---|---|---|
| DEVICE | Fully coated, removable , self-expanding oesophageal stent | Insertion 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.