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.
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