Endoscopic Ultrasound-Guided Gastroenterostomy Nationwide: Prospective Registry.
Recruiting now
Conditions studied: Endoscopic Surgical Procedure, Safety, Training
In brief
This is project of help and support for the introduction of the GASTROENTEROANASTOMOSIS technique guided by ENDOSCOPIC -ULTRASOUND (EUS-GE) in centers in Catalonia, facilitating a teacher training. The main objective is facilitate a safe introduction of the technique, limiting technical failures, and if necessary, support in rescue techniques. The goal of this interventional study is to assess the impact of a teaching and on live-support model in the introduction of the gastroenteroanastomosis technique, evaluating its effects in safety and the learning curve. regarding the results in safety and learning curve of for the introduction \[type of study: observational study or clinical trial\] is to \[learn about, test, compare etc.\] in \[describe participant population/health conditions\]. The main question\[s\] it aims to answer are: * \[question 1\] * \[question 2\] Participants will \[describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items\]. If there is a comparison group: Researchers will compare \[insert groups\] to see if \[insert effects\].
Key facts
- Study ID
- NCT05128604
- Run by
- Hospital Universitari de Bellvitge
- People needed
- 50
- Starts
- 2022-05-23
- Expected to finish
- 2026-09-24
- Last updated by the study team
- 2025-07-29
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18 years or more
- Gastric outlet obstruction (GOO) caused by passable /unpassable stenosis in the antrum-duodenal region, to malignant or non-malignant conditions
- Patient capable of understanding and signing informed consent form
- Patient understanding the type of study and complying with the follow-up of complementary tests during the study's duration
You may not qualify if…
- Massive ascites.
- Complete stenosis
- Failure to sign informed consent form
- Patients with intellectual handicap who are unable to understand the nature and possible consequences of the study, unless there is a competent legal representative
- Patients unable to adhere to subsequent follow-up requirements
- Severe coagulation disorder: INR > 1.5 not correctible with administration of plasma and/or platelets < 50,000/mm3
Where it is running
- Hospital Universitari Germans Trias i Pujol (Can Ruti) — Badalona, Barcelona, Catalonia, Spain (enrolling)
- Hospital Universitari de Bellvitge — L'Hospitalet de Llobregat, Barcelona, Catalonia, Spain (enrolling)
- Hospital Universitari Mútua de Terrassa — Terrassa, Barcelona, Catalonia, Spain (enrolling)
- Hospital de la Santa Creu i Sant Pau — Barcelona, Barcelona, Spain (enrolling)
- Hospital Del Mar — Barcelona, Catalonia, Spain (enrolling)
- Hospital Universitari de Girona Doctor Josep Trueta — Girona, Catalonia, Spain (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.