Bougie CAP in the treatment of benign oesophagus stenosis: randomised controlled pilot study

Not Applicable

• Conditions: K22.2; K20; K21.0; K91.83; Q39; Q87; T28.6; Oesophageal obstruction; Oesophagitis; Gastro-oesophageal reflux disease with oesophagitis

• Registration Number: DRKS00018996
• Lead Sponsor: Klinik für Kinder- und Jugendmedizin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-10-14
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Age below 18 years with benign Stenosis and informed consent of the parents

Exclusion Criteria

Missing informed consent, untreatable Stenosis

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
successful opening of the stricture and passing though (yes or no)

Secondary Outcome Measures

Name	Time	Method
QoL-Analysis (Sibergliet A. et al The dysphagia handicap index) before treatment, 1 and 14 days after treatment, Dysphagia-Score (BODS-2 Questionnaire) before treatment, 1 and 14 days after treatment, Duration of intervention (in minutes), need for change to another interventional method (Yes/No; and which), duration of Sedation (in minutes)