CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 7 enrolled
Drug / intervention
Tissue Apposition System (TAS) Devicedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00553436
NCT00553436N/ACompleted
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Evaluation of an Endoscopic Suturing System for Tissue Apposition in Colonic Polypectomy

Ethicon Endo-Surgery·interventional·Posted Nov 5, 2007·Updated Apr 27, 2010

In Brief

A clinical study evaluating Tissue Apposition System (TAS) Device for Polyps. Completed, enrolled 7 participants across 1 site.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPolyps
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedNov 5, 2007
Enrollment StartNov 1, 2007
Primary CompletionApr 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 18.7 years ago

Interventions

Tissue Apposition System (TAS) Devicedevice

Closure of defect following polypectomy using the Tissue Apposition System (TAS) Device.