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Evaluation of the PillCam™ Colon Capsule Endoscopy (PCCE) Night Procedure

Phase 3
Completed
Conditions
Colonic Diseases
Interventions
Device: PillCam™ (Capsule Endoscopy)
Registration Number
NCT00951587
Lead Sponsor
Medtronic - MITG
Brief Summary

The purpose of this study is to evaluate the effect of the night procedure in regards to colon cleansing level and capsule excretion rate.

Detailed Description

The evaluation of subjects with suspected colonic disease includes endoscopic imaging by colonoscopy and radiologic imaging such as air-contrast barium enema, or CT colonography. The Given® Diagnostic System offers an alternative approach for endoscopic visualization of the colon using capsule endoscopy, an ingestible device which contains imagers, light sources, a power source and a RF transmitter. Advantages of the Given® Diagnostic System include the elimination of the need for sedation, the minimally invasive, painless nature of the exam, and the ability to pursue normal daily activities immediately following the procedure . Furthermore, compared to standard colonoscopy, the Given® Diagnostic System may be more readily accepted by the subjects, thereby improving subjects' willingness to undergo a diagnostic evaluation of the colon and comply with colorectal cancer screening recommendations.

The PillCam™ SB capsule (formerly M2A® Capsule) that was FDA-approved in August 2001 for small bowel evaluation has been ingested to date by more than 500,000 people worldwide and is well accepted by patients and physicians as well as the processional societies. However, adequate visualization of the colon cannot be achieved with the standard PillCam™ SB capsule because of the anatomical and physiological properties of the colon which are significantly different than the small bowel. Moreover, other issues that limit the evaluation of the colonic mucosa by the standard PillCam™ SB procedure include an unsatisfactory level of colon cleanliness and slow progression of the PillCam™ SB capsule through the colon during the desired examination time. Therefore, the development and introduction of a specially designed, customized colon capsule combined with a dedicated capsule colonoscopy procedure protocol will allow for more efficient evaluation of the colonic mucosa. This is expected to improve the capability of the Given® Diagnostic System to detect colonic pathologies and to serve as a diagnostic and screening tool for colonic disease. Further details of the PillCam™ Colon Capsule Endoscope (PCCE) can be found in the device description section.

This is a pilot study that is designed to evaluate the level of cleanliness and visualization of colon achieved by colon capsule endoscopy when using Night procedure regimens for preparation of the colon.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
49
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
1PillCam™ (Capsule Endoscopy)Patients that are indicated for colonoscopy or who are suspected or known to suffer from colonic diseases.
Primary Outcome Measures
NameTimeMethod
Colon cleansing level scorewithin 7 days
Transit time in the different GI regions until excretionwithin 7 days
Secondary Outcome Measures
NameTimeMethod
Accuracy parameters of PCCE, compared to colonoscopywithin 7 days
Number of complete capsule procedurewithin 7 days
Patient subjective assessment questionnaireswithin 7 days

Trial Locations

Locations (2)

Berufsgenossenschaftliche Universitätskliniken Bergmannsheil

🇩🇪

Bochum, Germany

Knappschaftskrankenhaus Medizinische Universitaetsklinik

🇩🇪

Bochum, Germany

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