Spiral endoscopy for incomplete colonoscopy

• Conditions: 10018012; colon diseases

• Registration Number: NL-OMON35114
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 25

Inclusion Criteria

1) Adult patient 18 years-old or older
2) Able to read/write in Dutch
3) Previously attempted colonoscopy that failed to reach cecum
4) Previously attempted ileocolonscopy that failed to intubate the terminal ileum for patients with suspected Crohn*s disease.

Exclusion Criteria

1) Age < 18 years
2) Unable to provide informed consent

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint is the proportion of subjects with complete colon<br /><br>examination to the cecum using spiral colonoscopy. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoints include endoscopic procedural data including time-to-cecum,<br /><br>total procedural time, rate of terminal ileal intubation, endoscopic diagnostic<br /><br>yield, data regarding safety and adverse events, and patient tolerability data<br /><br>assessed using a comfort/discomfort visual analogue scale. </p><br>