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Clinical Outcomes of the Endoscopic Resection of Premalignant and Malignant Gastrointestinal Lesions

C

California Pacific Medical Center Research Institute

Status

Enrolling

Conditions

Benign Neoplasm of Intestinal Tract
Gastrointestinal Neoplasms

Study type

Observational

Funder types

Other

Identifiers

NCT01750619
2011.090

Details and patient eligibility

About

To evaluate clinical outcome for patients receiving treatment of suspected premalignant and malignant gastrointestinal lesions at Interventional Endoscopy Services. The primary outcome is curative endoscopic resection. Secondary outcomes include resection technique utilized, rates of en bloc resection and adverse event rates, including infection, bleeding, perforation and death, and one-year survival rates.

Enrollment

4,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients age >18 years that have been referred for endoscopic treatment of GI lesions.

Exclusion criteria

  • Patients for whom endoscopic treatment was not performed.

Trial design

4,000 participants in 3 patient groups

Mucosal tumors of the colon
Description:
Patients who received endoscopic treatment for noninvasive mucosal tumors of the colon.
Nonampullary tumors of the duodenum
Description:
Patients who received endoscopic treatment for noninvasive mucosal tumors of the duodenum.
Ampullary tumors
Description:
Patients who received endoscopic treatment for noninvasive ampullary tumors.

Trial contacts and locations

1

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Central trial contact

Jona C Bernabe

Data sourced from clinicaltrials.gov

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