EUS-directed Transenteric ERCP (EDEE) in Patients With Benign and Malignant Underlying Conditions and Inaccessible Papilla/Biliodigestive Anastomosis (BDA)

Recruiting N/A Interventional Study
Biliary Intervention Altered Anatomy Malignant Gastric Outlet Obstruction EUS Guided Enteroenteric Anastomosis EDEE
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
40 (estimated)
Sponsor
Evangelisches Krankenhaus Düsseldorf · Other
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About This Trial

Safety and efficacy of EDEE (EUS-directed transenteric ERCP)

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * signed consent form * Indication for an EDEE * Age \>18 years Exclusion Criteria: * Age \< 18 years
Contacts

Carina Friesl

+49 211 919 2171

carina.friesl@evk-duesseldorf.de

CONTACT

Leonie Dr. med. Grossmann

+49 211 919 1605

Leonie.Grossmann@evk-duesseldorf.de

CONTACT