Rétrospective Evaluation of the Performance and the Safety of the Endoscopic Mucosectomy With Anchorage

Sponsor
Hôpital Edouard Herriot (Other)
Overall Status
Completed
CT.gov ID
NCT03467451
Collaborator
(none)
125
30.1

Study Details

Study Description

Brief Summary

This safe and simple technique without extra cost would allow us to improve R0 resection ratio and so decrease relapses and the time between two different exams

Condition or Disease Intervention/Treatment Phase
  • Procedure: Endoscopic Mucosectomy

Study Design

Study Type:
Observational
Actual Enrollment :
125 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Rétrospective Evaluation of the Performance and the Safety of the Endoscopic Mucosectomy With Anchorage of the Tip of the Loop
Actual Study Start Date :
Jul 1, 2015
Actual Primary Completion Date :
Jul 1, 2016
Actual Study Completion Date :
Jan 1, 2018

Outcome Measures

Primary Outcome Measures

  1. Measure the proportion of R0 resections of anchored mucosectomies from 10 to 30 mm colon and rectum lesions [One year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 85 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Age over 18 years old

  • Other rectal or colic résections from 10 to 30 mm into the past

Exclusion Criteria:
  • Colitis, Crohn Disease or Ulcerative Colitis

  • Intense fibrosis under the lesion

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Hôpital Edouard Herriot

Investigators

  • Principal Investigator: Mathieu Pioche, Edouard Herriot Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jean Christophe Saurin, Professor, Société Française d'Endoscopie Digestive
ClinicalTrials.gov Identifier:
NCT03467451
Other Study ID Numbers:
  • Mucosectomy with anchorage
First Posted:
Mar 16, 2018
Last Update Posted:
Mar 19, 2018
Last Verified:
Mar 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 19, 2018