CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 20 enrolled
Drug / intervention
Mesh Implantationdevice
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/NCT03750461
NCT03750461N/ACompleted

Stoma Closure and Reinforcement (SCAR) Trial - A Single Center Pilot Study of the Safety of a Mesh Reinforcement of Ileostomy Closure to Prevent Hernia Formation in Left Sided Colon and Rectal Cancer Patients

Dartmouth-Hitchcock Medical Center·interventional·Posted Nov 23, 2018·Updated Feb 22, 2023

In Brief

A clinical study evaluating Mesh Implantation for Colon Cancer and 2 related conditions. Completed, enrolled 20 participants across 1 site.

Detailed Summary

Hernia formation at sites of ostomy closure is a common complication. The investigator believes that using evidence based hernia repair techniques as a preventive measure during closure of ostomies will reduce the incidence of hernia formation. In this trial, the investigator will pilot a novel technique of large pore monofilament polypropylene mesh reinforcement of the abdominal wall defects that remain after closure of an ileostomy to evaluate for safety and begin to evaluate the effectiveness compared to standard techniques.

Study Details

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

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedNov 23, 2018
Enrollment StartJan 1, 2019
Primary CompletionJan 30, 2021
Study CompletionFeb 1, 2023
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 7.6 years ago

Interventions

Mesh Implantationdevice

Implantation of permanent mesh (BARD Soft Mesh) into the abdominal wall for reinforcement to prevent hernia formation