NBI Versus White Light Endoscopy for Optical Characterization of Neoplastic Polyps in the Colorectum

NCT ID: NCT03679429

Last Updated: 2018-09-20

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

UNKNOWN

Total Enrollment

370 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-11-30

Study Completion Date

2020-07-31

Brief Summary

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Adenomas, serrated adenomas and hyperplastic polyps are polypoid lesion in the colorectum. At the present moment, all polyps should be resected endoscopically, although only adenomas and serrated adenomas, but not hyperplastic polyps have the potential to develop colorectal cancer. This approach enables the conduction of microscopic investigations of the lesions. By today, only the pathological diagnosis can distinguish exactly between these three polyp entities. Some studies have investigated the value of the optical characterization approach which is based on visual assessment of the polyp' surface structures. Based upon optical polyp features users are encouraged to predict histopathological polyp diagnoses solely on behalf of optical or endoscopical criteria. This method is conducted in real time during colonoscopy. If it could be shown, that endoscopist using the optical characterization approach are able to predict histopathological diagnoses of colonic polyps sufficiently this would possibly lead to simplification of diagnostic procedures. For instance, it would be conceivable to resect small polyps and discard them without further assessment by a pathologist. One problem in this context is a correct differentiation between hyperplastic polyps and serrated adenomas. These two polyp entities are known to show similar optical features. However, while serrated adenomas are premalignant lesions hyperplastic polyps have benign histology and never develop into cancer. It is therefore important to sufficiently distinguish hyperplastic polyps from serrated lesions.

In this study we want to investigate whether the use of narrow-band imaging (NBI) would be capable to rise accuracy of optical polyp predictions compared to standard HD white light endoscopy. NBI is a light filter tool which can be activated by pressing a button at the endoscope. The use of NBI leads to an endoscopic picture which appears blue and enables endoscopists to better assess surface structures and vascular patterns.

In a prospective randomised multicenter setting we plan to conduct colonoscopy in 370 patients. Half of the patients will be examined without the use of NBI (control arm). In these cases colonoscopists will assess optical diagnosis of polyps without turning on the NBI tool. If polyps are detected in patients belonging to the intervention arm NBI will be used and optical diagnosis will be determined using the WASP (Workgroup serrAted polypS and Polyposis) classification. All polyps will be resected and send to pathology for further microscopic assessment. After completing the trial we aim to compare accuracy of the optical diagnosis in both groups. Our hypothesis is, that by using NBI accordance between optical and histopathological diagnosis can be increased from 80% to 90%.

Detailed Description

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Conditions

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Colon Adenoma Colorectal Carcinoma Hyperplastic Polyp Serrated Adenoma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Control group

Patients from the control group will be examined using a CF-HQ 190 EVIS Exera III Advanced Diagnostic Video Colonoscope. If colon polyps are detected optical diagnosis will be determined WITHOUT using the NBI function of the scope.

No interventions assigned to this group

Intervention

Patients from the control group will be examined using a CF-HQ 190 EVIS Exera III Advanced Diagnostic Video Colonoscope. If colon polyps are detected optical diagnosis will be determined by using the NBI function of the scope.

NBI Function

Intervention Type DEVICE

In the intervention arm polyps will be optically characterized using the NBI function. The WASP (Workgroup serrAted polypS and Polyposis) classification will be used in order to determine the optical diagnosis.

Interventions

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NBI Function

In the intervention arm polyps will be optically characterized using the NBI function. The WASP (Workgroup serrAted polypS and Polyposis) classification will be used in order to determine the optical diagnosis.

Intervention Type DEVICE

Other Intervention Names

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NBI Function integrated in the CF-HQ 190 EVIS Exera III Advanced Diagnostic Video Colonoscope

Eligibility Criteria

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Inclusion Criteria

* medical indication for colonoscopy
* age ≥ 40 years
* written consent given by patient

Exclusion Criteria

* age \< 40 years
* patients denying written consent
* pregnant women
* ASA class IV, V and VI
* known contraindication for polyp resection
* indication for colonoscopy: preknown adenoma/polyp/carcinoma or inflammatory bowel disease
* indication for colonoscopy: emergency (e.g. severe rectal bleeding)
Minimum Eligible Age

40 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Technical University of Munich

OTHER

Sponsor Role lead

Responsible Party

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Peter Klare

Dr. med. Peter Klare

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Peter Klare, MD

Role: PRINCIPAL_INVESTIGATOR

Klinikum rechts der Isar der Technischen Universität München

Roland M Schmid, Professor

Role: STUDY_DIRECTOR

Klinikum rechts der Isar der Technischen Universität München

Timo Rath, Professor

Role: STUDY_CHAIR

Universitätsklinikum Erlangen

Jan Peveling-Oberhag, MD

Role: STUDY_CHAIR

Robert Bosch-Krankenhaus Stuttgart

Locations

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Klinik für Innere Medizin II am Klinikum rechts der Isar der Technischen Universität München

Munich, Bavaria, Germany

Site Status

Universitätsklinikum Erlangen, Medizinische Klinik 1

Erlangen, , Germany

Site Status

Robert-Bosch-Krankenhaus

Stuttgart, , Germany

Site Status

Countries

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Germany

Central Contacts

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Peter Klare, MD

Role: CONTACT

+49 89 4140 9340

Facility Contacts

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Peter Klare, MD

Role: primary

+49 89 4140 9340

Timo Rath, Professor

Role: primary

Jan Peveling-Oberhag, MD

Role: primary

Other Identifiers

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ADOPTION II

Identifier Type: -

Identifier Source: org_study_id

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