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Endoscopical Dilation of Benign Esophageal Strictures

NCT01738997 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2012-11-30

No results posted yet for this study

Summary

Although balloon dilatation is the primary treatment for benign dysphagia, information about the optimal inflation time is lacking. The aim of the current pilot study was to compare 10 seconds inflation time, with 2 minutes inflation time, regarding the efficacy

Conditions

Interventions

DEVICE

Dilation 10 sec

DEVICE

Dilation 2 min

Sponsors & Collaborators

  • Uppsala University

    collaborator OTHER

  • Boston Scientific Corporation

    collaborator INDUSTRY

  • University Hospital, Umeå

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-12-31
Primary Completion
2006-12-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01738997 on ClinicalTrials.gov