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Clinical Trials/JPRN-UMIN000050513
JPRN-UMIN000050513
Recruiting
N/A

An observational study to evaluate the efficacy of suturing mucosal defects post duodenal endoscopic submucosal dissection - Suturing study post duodenal ESD

Keio University0 sites220 target enrollmentMarch 7, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
superficial non-ampullary duodenal epithelial tumor
Sponsor
Keio University
Enrollment
220
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 7, 2023
End Date
March 31, 2027
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\) Patients with familial adenomatous polyposis (FAP) (2\) Patients who are treated for multiple lesions at the same time (patients with multiple lesions, including those of other organs, can be included if only one lesion is treated during the protocol treatment period) (3\) Patients with history of duodenal resection in the past (4\) Patients with a distance of 10 mm or less between the lesion and the duodenal papilla or accessory papilla (5\) Patients whose lesions involve the duodenal bulb on the oral side (6\) Vital organ insufficiency (heart, lung, liver, kidney, bone marrow) (7\) Patients who cannot be managed perioperatively with antithrombotic drugs according to the guidelines proposed by Japan Gastroenterological Endoscopy Society (8\) Other patients considered by the attending physician to be ineligible for entry

Outcomes

Primary Outcomes

Not specified

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