The effect of endoscopic treatments in the treatment of benign esophageal stricture

Phase 3

Recruiting

• Conditions: benign esophageal stricture.; Esophageal obstruction; K22.2

• Registration Number: IRCT20230425057990N2
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 75

Inclusion Criteria

Unable to swallow
Difficulty to swallow
Benign esophageal stricture secondary to caustic injury

Exclusion Criteria

achalasia
Untreated reflex
Esophageal surgery during the last month
Patients needing surgery

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Technical success. Timepoint: Before the intervention, one month, three months and six months after the intervention. Method of measurement: Based of lumen diameter with residual stenosis less than 30%.;Technical success. Timepoint: Before the intervention, one month, three months and six months after the intervention. Method of measurement: Improvement of dysphagia symptoms.

Secondary Outcome Measures

Name	Time	Method
Generic Quality of life. Timepoint: Before the intervention, one month, three months and six months after the intervention. Method of measurement: EuroQol-5D (EQ-5D) index.;Physically quality of life. Timepoint: Before the intervention, one month, three months and six months after the intervention. Method of measurement: body mass index.;Complication. Timepoint: up to 6 hours after the intervention. Method of measurement: Physical examination and history.