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Multicenter prospective trial of colonoscopy using short length double balloon endoscopy for patients with previous incomplete colonoscopy

Not Applicable
Conditions
Colorectal disease
Registration Number
JPRN-UMIN000003464
Lead Sponsor
DBC study group
Brief Summary

A total of 110 patients (62 males, median age 66.5 years) were included. Fifty-four patients had a history of abdominal surgery. The cecal intubation rate was 100% (110/110). Median intubation time was 12 minutes (range 4-47 minutes). Mild mucosal tears without symptoms occurred in 1 patient. For 64.5% of patients, intravenous sedatives and/or analgesics were used during examinations. Based on questionnaires, 50.9% had no pain, 31.8% slight pain, and 17.3% tolerable pain. Moreover, 96.4% of patients answered that their examination was more comfortable than their previous colonoscopy.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
110
Inclusion Criteria

Not provided

Exclusion Criteria

Past history of colorectal surgery Insufficient preparation GI polyposis syndrome IBD Pregnancy On-going GI obstruction On-going GI bleeding Severe heart or respiratory failure Dementia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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