Colon Cancer Clinical Trial

Improving Complete Endoscopic Mucosal Resection (EMR) of Colorectal Neoplasia

Summary

The investigators seek to compare two techniques of removing pre-cancerous lesions from the colon. The investigators also will compare two solutions used during the procedure to determine if either solution allows for an improved removal of the tumors.

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Full Description

The primary aim of the study is to compare the efficacy, efficiency and safety of two types of snares used in Endoscopic Mucosal Resection (EMR), a combined needle and snare unit (ISnare, US Endoscopy) versus an oval braided snare with spiral wire (Snaremaster, Olympus). The secondary aim is to explore whether EMR efficacy and efficiency is depended upon the injection solution used, saline versus Gonak (a solution containing HPMC, saline, and epinephrine) for EMR.

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Eligibility Criteria

Inclusion Criteria:

Sessile colorectal polyp
laterally spreading lesions as defined by Paris Classification type II and > 1 cm or greater

Exclusion Criteria:

Those with ulcerated depressed lesions (Paris type III) or biopsy proven invasive carcinoma
Inflammatory bowel disease patients
Coagulopathy ( INR> 1.5) that cannot be corrected

Study is for people with:

Colon Cancer

Phase:

Phase 4

Estimated Enrollment:

66

Study ID:

NCT01471756

Recruitment Status:

Completed

Sponsor:

Mayo Clinic

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There is 1 Location for this study

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Mayo Clinic
Jacksonville Florida, 32224, United States

How clear is this clinincal trial information?

Study is for people with:

Colon Cancer

Phase:

Phase 4

Estimated Enrollment:

66

Study ID:

NCT01471756

Recruitment Status:

Completed

Sponsor:


Mayo Clinic

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