MedTrace Logo

Balloon Colonoscopy for Incomplete Colonoscopy

NCT00935857 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2014-09-25

Study results available
· View outcomes & findings →

Summary

Patients with a prior incomplete colonoscopy will be enrolled in this study. Patients will be randomized to either an initial repeat attempt with a standard colonoscope or the single balloon enteroscope. If the procedures is unsuccessful, the patient can be crossed-over to the other group. The primary endpoint of the study is a complete colonoscopy.

Conditions

  • Diverticulosis

Interventions

DEVICE

Single Balloon Colonoscopy

Use of the single balloon enteroscopy system (enteroscope and balloon-overtube) to complete colonoscopy.

DEVICE

Standard Colonoscopy

Use of the standard adult colonoscope to complete colonoscopy.

Sponsors & Collaborators

Principal Investigators

  • Rajesh N Keswani, MD · Northwestern University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2009-04-30
Primary Completion
2010-12-31
Completion
2010-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

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 NCT00935857 on ClinicalTrials.gov