Evaluation of the Main Determinants of Patient Acceptability of the Bowel Cleansing Procedure, and of Success of Bowel Cleansing and Caecal Intubation

NCT ID: NCT01626196

Last Updated: 2012-07-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

600 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-02-29

Study Completion Date

2012-06-30

Brief Summary

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Several factors are important in achieving a successful colonoscopy, including patient acceptability of the bowel cleansing procedure and the overall quality of cleansing.

This observational study has been designed to explore the main determinants of acceptability of the bowel cleansing procedure to the patient in an Italian "real life" setting. In addition, the study is to examine the determinants of quality of bowel cleansing and describe aspects of the technical performance of the colonoscopy (time to reach the caecum and adenoma detection rate).

Detailed Description

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Conditions

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Routine Colonoscopy

Study Design

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Observational Model Type

ECOLOGIC_OR_COMMUNITY

Study Time Perspective

PROSPECTIVE

Study Groups

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Colonoscopy patients

Patients undergoing with bowel cleansing procedures according to the clinics' usual routine

No intervention

Intervention Type OTHER

This was an observational study

Interventions

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No intervention

This was an observational study

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Written informed consent obtained prior to inclusion.
* Male and female outpatients, aged ≥ 18, treated with bowel cleansing preparation the day before undergoing routine colonoscopy at selected participating centres.

Exclusion Criteria

* Children and adolescents aged less than 18 years. Pregnant or breastfeeding women.
* Listed contra-indications to the relevant product used for the bowel cleansing procedure.
* Patients having been submitted to a previous colonoscopy over the last five years.
* Patients who have taken laxative enemas the day preceding the colonoscopy.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Norgine

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Alessandro Repici, MD

Role: PRINCIPAL_INVESTIGATOR

Instituto Clinico Humanitas

Locations

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IRCCS Instituto Clinico Humanitas

Milan, Rozzano, Italy

Site Status

Countries

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Italy

Other Identifiers

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NIT MOV 1002

Identifier Type: -

Identifier Source: org_study_id