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Colonoscopy clinical trials

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NCT ID: NCT01055782 Completed - Pain Clinical Trials

Colonoscopy Endoguide in Specialist Practice

Start date: November 2009
Phase: N/A
Study type: Interventional

The study includes 700 patients referred for colonoscopy are randomized to colonoscopy with or without endoguide. The study will investigate whether the endoguide improves success rate and the patient's perception of pain.

NCT ID: NCT00988676 Completed - Colonoscopy Clinical Trials

The Effect of Bowel Preparation Status on the Polyp Missing Rate

Start date: May 2009
Phase: N/A
Study type: Observational

High quality bowel cleaning preparation was most important prerequisites of a accurate colonoscopy, because even a small amount of residual fecal matter can obscure small polyps and increase unnecessary procedure time. Until now, several studies evaluated the impact of bowel preparation on the quality of colonoscopy using comparison of the polyp detection rate in patients with adequate bowel preparation status to that in patients with inadequate bowel preparation status during colonoscopy. However, there was no direct measurement the effect bowel preparation status on the polyp missing rate, the quality of colonoscopy, using tandem colonoscopic evaluation in prospective setting.

NCT ID: NCT00975247 Completed - Colon Cancer Clinical Trials

Impact of a Novel Patient Educational Booklet on Colonoscopy Quality

Start date: April 2008
Phase: N/A
Study type: Interventional

Background: Achievement of colonoscopy outcomes depends on high-quality bowel preparation by patients; yet inadequate preparation is common. Objective: To develop and test an educational booklet to improve bowel preparation quality. Design: "Before-and-after" study followed by randomized controlled trial. Setting: Veteran Affairs medical center. Patients: Patients undergoing outpatient colonoscopy Measurements: The investigators first performed cognitive interviews to identify knowledge and belief barriers to high-quality colonoscopy preparation. The investigators then created a patient educational booklet addressing patient barriers to improve preparatory behaviors. The investigators tested the booklet in 2 sequential studies: (1) controlled "before-and-after" study in patients undergoing colonoscopy during 2 consecutive months: 1 without and 1 with the booklet; (2) randomized controlled trial. The outcome in both studies was bowel preparation quality measured on a 6-point Likert scale (>5="good"). In each study the investigators compared the proportion achieving a "good" preparation between groups and performed logistic regression to measure the effect of the booklet on preparation quality while adjusting for the purgative received. Limitations: Unknown impact on polyp yield and cancer reduction.

NCT ID: NCT00959491 Active, not recruiting - Colonoscopy Clinical Trials

A Prospective Study of a New Immunological Fecal Occult Blood Test

RLHV
Start date: October 2009
Phase: N/A
Study type: Observational

The purpose of the investigators study is to evaluate the diagnostic ability of a new immunological fecal occult blood test in Cuban patients undergoing colonoscopy .

NCT ID: NCT00953017 Completed - Colonoscopy Clinical Trials

A Trial Comparing Split-Dose Miralax With Amitiza Pretreatment Versus Dulcolax Pretreatment Versus Golytely for Bowel Cleansing Prior to Colonoscopy

Start date: July 2009
Phase: Phase 4
Study type: Interventional

Miralax (PEG 3350) has been shown to be a safe and uncomplicated bowel preparation prior to colonoscopy in pediatric populations. This study seeks to confirm the efficacy of this bowel cleansing regimen in adults and to determine the benefit of adding a pretreatment medication to this bowel preparation. The tolerability of Miralax will hopefully improve patient satisfaction with colonoscopy and decrease their reluctance to be screened because of the uncomfortable taste and side effects of bowel preparation regimens.

NCT ID: NCT00930462 Completed - Colonoscopy Clinical Trials

Evaluation of the Use of Cap in Improving the Performance of Colonoscopy

Start date: March 2008
Phase: Phase 4
Study type: Interventional

The aim of this study is to compare the colonoscopy success rate, cecal time and polyp detection rate between cap-fitted colonoscopy and conventional colonoscopy.

NCT ID: NCT00929916 Completed - Colonoscopy Clinical Trials

Comparing Two Different Ways to Take MoviPrep® Before Colonoscopy

Start date: December 2008
Phase: N/A
Study type: Observational

This study will evaluate whether morning-only dosing of MoviPrep® (2L) for afternoon colonoscopy is as effective as a standard dosing regimen of half of the volume of MoviPrep® (1L) solution the evening prior, and half (1L) the morning of, colonoscopy. MoviPrep® is a low volume (2 liters) polyethylene glycol (PEG)-based purgative that is approved for evening-only or split (evening and morning) dosing to cleanse the colon prior to colonoscopy. Patients undergoing afternoon colonoscopies often have inferior colon cleansing. There is evidence that morning-only purgative administration of large volume PEG (4L) is safe and effective. This study will assess whether administration of a low volume PEG regimen will maintain efficacy and improve tolerance by changing a 2-day preparation procedure into a regimen that is completed in 1 day.

NCT ID: NCT00913861 Terminated - Colonoscopy Clinical Trials

Non-pharmacological Intervention for Colonoscopy

Start date: May 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a non-pharmacological intervention reduces consumption of sedative drugs during colonoscopy. A reduction of sedative drugs may reduce side effects. This non-pharmacological intervention may increase patient's comfort and security.

NCT ID: NCT00908648 Completed - Colonoscopy Clinical Trials

The Use of Narrow Band Imaging in Screening Colonoscopy

Start date: November 2007
Phase: N/A
Study type: Interventional

Narrow band imaging (NBI) is an imaging technique that allows a better definition of capillary pattern and improves the contrast between adenomas and the surrounding mucosa. Conflicting data exist on the ability of NBI in to improve detection of colonic neoplasm; the impact of NBI is being tested in several screening scenarios. The investigators evaluated whether the routine use of NBI, compared to white light (WL), during the withdrawal phase of screening colonoscopy improved adenoma detection.

NCT ID: NCT00905554 Completed - Colonoscopy Clinical Trials

Warm Water for Unsedated Colonoscopy

WW
Start date: April 2009
Phase: N/A
Study type: Interventional

Unsedated colonoscopy is characterized by lower costs, recovery time and incidence of drug-related side effects, although it may be painful for the patient. Based on recent reports, the investigators designed this randomized controlled trial hypothesizing that the use of water irrigation versus air insufflation during the insertion phase of colonoscopy might increase the global tolerability of the examination and the proportion of patients undergoing complete colonoscopy without sedation.