Endoscopic Resection Multicenter Registry

NCT03065257 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2017-04-25

No results posted yet for this study

Summary

This is a retrospective and prospective multicenter registry to collect long-term data (1 year) on patients who have or will undergo Endoscopic resection such as EMR, ESD, EFTR, STER, etc. within the gastrointestinal tract for endoscopic treatment of early gastrointestinal neoplasms involving the resection of the superficial layers, mucosa and submucosa, of the tract wall.

Subjects will be consented for medical chart review.

The purpose of this retrospective and prospective registry is to assess long term data on efficacy, safety and clinical outcome of Endoscopic Resection within the gastrointestinal tract (1 year).

The registry will evaluate efficacy, technical feasibility, clinical outcome, safety profile and overall clinical management through medical chart review. The procedures the investigators are evaluating are all clinically indicated and will not be prescribed to someone to participate in this registry study.

Conditions

  • Gastrointestinal Neoplasms
  • Gastrointestinal Disease
  • Gastric Cancer
  • Gastric Neoplasm
  • Gastric Polyp
  • Esophageal Neoplasms
  • Duodenal Neoplasms
  • Duodenal Polyp
  • Stomach Neoplasm
  • Stomach Polyp
  • Neoplasms
  • Colon Polyp
  • Colon Neoplasm

Interventions

PROCEDURE

Endoscopic Resection

Any Endoscopic resection for Gastrointestinal disorders including neoplasms.

Sponsors & Collaborators

  • Weill Medical College of Cornell University

    lead OTHER

Principal Investigators

  • Michel Kahaleh, MD · Weill Medical College of Cornell University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-03-15
Primary Completion
2020-03-31
Completion
2020-04-30

Countries

  • United States

Study Locations

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Entities

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 NCT03065257 on ClinicalTrials.gov