Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01200147

Effectiveness of Rupture of Schatzki's Ring Using Biopsy Forceps Versus SIngle Dilation

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Nova Scotia Health Authority · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Dysphagia is a common reason for referal to the investigators Gastoenterology service. As many as 14% of patients undergoing radiological studies for dysphagia are found to have schatzki rings. Current recommendations for treatment of patients with symptomatic Schatzki rings are based on ancedotal experience and uncontrolled studies. The only randomized study on comparison of techniques the investigators were able to locate was published in 2000 and included only 26 patients. This study demonstrated that the biopsy techinque was as effective as and better tolerated than the standard dilation technique. Considering that the cost and time required for dilatation is greater than the basic biopsy technique, significant cost savings could be achieved using the biopsy technique. As well, patient satisfaction is an important factor considering that Schatzki rings can recur and repeated endoscopy is often required. Therefore, a study that shows a technique to be as or better than the current standard in effectiveness, cost, time, and patient comfort could lead to shift in current practice.

Detailed description

None available, study was withdrawn

Conditions

Interventions

TypeNameDescription
OTHERstudy withdrawn no details

Timeline

Start date
2010-09-01
Primary completion
2010-09-01
Completion
2010-09-01
First posted
2010-09-13
Last updated
2022-11-08

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01200147. Inclusion in this directory is not an endorsement.