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A RETROspective Data Collection of comPRESSion Anastomosis Using the ColonRing

NCT01880918 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2013-06-19

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 4-6 centers. The data will assist in future evaluating the performance of the ColonRing device in regards to the creation of a colorectal anastomosis in Low Anterior Resection procedures.

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

Sponsors & Collaborators

  • novoGI

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2013-06-30
Completion
2013-07-31

Countries

  • United States

Study Locations

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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 NCT01880918 on ClinicalTrials.gov