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Clinical Trials/NCT03604237
NCT03604237UnknownNot Applicable

Concordance Rate of Pathology Between Targeted Forceps Biopsy and Resected Specimen for Large Colorectal Tumors

Kyungpook National University Hospital1 site in 1 country64 target enrollmentStarted: September 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
64
Locations
1
Primary Endpoint
pathologic diagnosis

Study Overview

Brief Summary

This study evaluates whether targeted forceps biopsy with careful tumor surface evaluation can improve diagnostic accuracy of colorectal tumors larger than 2 cm during colonoscopy.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
19 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients with colorectal neoplasms of the size larger than 2 cm

Exclusion Criteria

  • •Patients who deny the participation in the study

Arms & Interventions

Targeted forceps biopsy

Experimental

In this group, an endoscopist takes a forceps biopsy at depressed mucosa or large nodular area of large colorectal tumors after meticulous surface evaluation.

Intervention: Targeted group (Diagnostic Test)

Conventional forceps biopsy

No Intervention

In this group, an endoscopist takes a forceps biopsy at the most convenient area of large colorectal tumors.

Outcomes

Primary Outcomes

pathologic diagnosis

Time Frame: 7 days

The pathologic diagnosis of forceps biopsy is compared with the pathologic diagnosis of resected specimen of the colorectal tumor.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Eun Soo Kim, MD, PhD

Professor

Kyungpook National University Hospital

Study Sites (1)

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