Skip to content

Endoscopic Resection Multicenter Registry

Endoscopic Resection: A Retrospective and Prospective Multicenter Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03065257
Enrollment
200
Registered
2017-02-27
Start date
2017-03-15
Completion date
2020-04-30
Last updated
2017-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

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

Keywords

EMR, ESD, Resection, STER, EFTR, Submucosal dissection, Endoscopic resection

Brief 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.

Detailed description

Endoscopic resection can be an appropriate approach in early neoplasms, challenging adenomas or sub-epithelial lesions. Endoscopic resection can be considered as a less invasive approach than surgery. Moreover, endoscopic resection can be available to patients who are ineligible for surgery or who have refused more aggressive surgical intervention. The study investigators would collect data on a large sample size of subjects undergoing various endoscopic resection procedures such as EMR (Endoscopic Mucosal Resection), ESD (Endoscopic submucosal dissection), STER (Submucosal tunneling endoscopic resection, and EFTR (Endoscopic full-thickness resection). Clinical metrics will be recorded including procedure times, length of follow-up, specific tumor characteristics, resection method, pathology results, procedural complications, additional therapy required, and disease-free survival time. Currently, there is limited multi-center data on endoscopic resection outcomes in western populations. Evaluation of these measurement would help the investigators compare them to conventional treatment modalities within current tertiary facilities; and consequently help the investigators identify appropriate treatment techniques and improve clinical management of patients at WCMC-NYPH. 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).

Interventions

Any Endoscopic resection for Gastrointestinal disorders including neoplasms.

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Any patient who is considering undergoing endoscopic resection within 6 months, or has undergone clinically indicated endoscopic resection within the past 6 months * Above or equal to 18 years of age.

Exclusion criteria

* Any patient who has not undergone or will undergo endoscopic resection * Below 18 years of age.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with reduction in clinical symptoms6 months from procedureTo assess resolution of symptoms of all Endoscopic resection procedures at 6 months

Secondary

MeasureTime frameDescription
Number of participants with treatment-related adverse events as assessed by CTCAE v4.030 days post procedureNumber of subjects with Adverse Events; Type, frequency and intensity of adverse events within 30 days of procedure

Other

MeasureTime frameDescription
Number of participants with successful completion of treatment30 days post procedureNumber of participants with successful completion of treatment

Countries

United States

Contacts

Primary ContactMichel Kahaleh, MD
mik9071@med.cornell.edu646-962-4797
Backup ContactMonica R Gaidhane, MPH
mog2012@med.cornell.edu646-962-4796

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026