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Data Collection of Patients Treated With the ColonRing™ for the Creation of Circular Compression Anastomosis

NCT01301417 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 171

Last updated 2013-06-05

No results posted yet for this study

Summary

The proposed study is a post marketing, observational, retrospective data collection intended to gather and record data on patients treated with the ColonRing™ device in routine clinical practice at a single center. The data will assist in further evaluating the performance of the ColonRing™ device in regards to the creation of a colorectal anastomosis.

Hypothesis:The performance of the ColonRing™, determined by the rate of complications, will be within the acceptable range reported in the literature for alternative treatment modalities.

Conditions

  • Diverticulum, Colon
  • Colorectal Neoplasms
  • Crohn Disease
  • Colitis, Ulcerative
  • Colostomy
  • Ileostomy - Stoma
  • Rectal Prolapse
  • Intestinal Polyposis
  • Lymphoma
  • Endometriosis
  • Intestinal Volvulus

Interventions

DEVICE

ColonRing™

Creation of a circular Compression Anastomosis

Sponsors & Collaborators

  • novoGI

    lead INDUSTRY

Principal Investigators

  • Eran Choman, Msc · novoGI

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2011-08-31
Completion
2011-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT01301417 on ClinicalTrials.gov