COMPRES - COMpression Anastomosis Ring (CAR™ 27/ColonRing™) Post maRketing Evaluation Study

NCT01091155 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 288

Last updated 2013-10-25

Study results available
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Summary

The performance of the ColonRing™ will be comparable to or better than the reported performance of staplers.

Conditions

  • Colorectal Surgery

Interventions

DEVICE

ColonRing (Colorectal anastomosis)

Creation of a colorectal compression anastomosis

Sponsors & Collaborators

  • Atlanta Colon & Rectal Surgery, Atlanta, GA

    collaborator OTHER
  • FPMG Center for Colon & Rectal Surgery

    collaborator UNKNOWN
  • Lester E. Cox Medical Centers

    collaborator OTHER
  • UCI Medical Center Irvine CA

    collaborator UNKNOWN
  • Endeavor Health

    collaborator OTHER
  • St.Louis University hospital MO

    collaborator UNKNOWN
  • University of Southern California

    collaborator OTHER
  • Bnai Zion Medical Center

    collaborator OTHER_GOV
  • Barmherzig Brueder

    collaborator UNKNOWN
  • Catharina Ziekenhuis Eindhoven

    collaborator OTHER
  • Ziekenhuis Oost-Limburg

    collaborator OTHER
  • University Hospital, Gasthuisberg

    collaborator OTHER
  • Klinikum Neuperlach

    collaborator UNKNOWN
  • novoGI

    lead INDUSTRY

Principal Investigators

  • Eran Choman, Msc · novoGI

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2011-07-31
Completion
2011-07-31

Countries

  • United States
  • Austria
  • Belgium
  • Germany
  • Israel
  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01091155 on ClinicalTrials.gov