Evaluation of an Endoscopic Suturing System for Tissue Apposition in Colonic Polypectomy

Ethicon

Status

Completed

Conditions

Polyps

Treatments

Device: Tissue Apposition System (TAS) Device

Study type

Interventional

Funder types

Industry

Identifiers

NCT00553436

UH IRB #07-07-08

CI-07-0004

Details and patient eligibility

About

The purpose of this study is to show that the surgical site in the bowel wall can be sewn closed in the colon or intestine, with a new sewing device after removal of a benign polyp according to standard of care.

Full description

Polypectomy is the medical term for removing polyps. Polyps are abnormal like growths that protrude into the lining of the bowel. Because a polyp cannot always be removed by a snare, the usual and simplest method, (for example, it may be too flat), a doctor (colorectal surgeon) may perform a polypectomy using a technique called Endoscopic Mucosal Resection (EMR). Endoscopic Mucosal Resection (EMR)is based on the concept that endoscopy (looking at the inside of your colon with an instrument called a colonoscope) provides visualization and access to the innermost lining of the gastrointestinal tract, where a polyp originates. The Endoscopic Mucosal Resection (EMR)performed during this study will be standard of care according to the current practice at University Hospitals of Cleveland.

Following polyp removal, the study procedure will be performed. A medical device is being evaluated to help with this procedure by closing the wound that remains after the polyp is removed without performing an open surgical operation. This involves suturing (sewing) the tissue back together with a Tissue Apposition System (TAS). This is also called tissue approximation. The sewing device being evaluated has been cleared by the Food and Drug Administration (FDA).

Up to 20 men and women, at least 21 years of age, requiring removal of a colonic or rectal polyp that cannot be removed by traditional colonic polypectomy, will be asked to enroll in the study. Following polyp removal, these patients will have the remaining tissue area closed using the study sewing device. Participation in this study will last approximately three months.

Enrollment

7 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

At least 21 years of age;
Willing to give consent and comply with evaluation and treatment schedule;
Approved for polypectomy per standard preoperative endoscopic evaluation;
Established indication for a procedure greater than colonoscopy and colonic polypectomy. This will include polyps not suitable for current practice (snare procedure) endoscopic resection by nature of size or location, in which an intestinal resection, laparoscopic-assisted polypectomy is required;
Surgical area viewable with laparoscopy.

Exclusion criteria

Physical or psychological condition which would impair study participation;
Unable or unwilling to attend follow-up visits and examinations;
Concurrent surgical procedure;
Pregnancy;
A polyp which appears to be an invasive cancer, even with negative pathology;
A polyp with biopsies suspicious for invasive cancer;
Participation in any other investigational device or drug study within 30 days prior to enrollment; or
Any condition which precludes compliance with the study.