Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 6:31 PM
Ignite Modification Date:
2025-12-24 @ 6:31 PM
NCT ID:
NCT02562157
Eligibility Criteria:
Inclusion Criteria:
* Age \> 18 years old
* Benign or malignant antropyloric or duodenal obstruction leaving free the 3rd and the 4th duodenum, confirmed by CT scan or endoscopy
* Patient having been hospitalized at least once for this indication, with failure of medical treatment and/or failure or impossibility of endoscopic treatment using metallic duodenal stenting.
* Patients having under nutrition with a weight loss \> 10%
* Theorical indication of surgical gastroenteric anastomosis with operating contraindication or refusal of the surgery by the patient
* Indication validated during multidisciplinary meeting
* GOOSS score = 0 or 1
* Patient having received clear and complete information and given written consent
* Patient having medical care insurrance
Exclusion Criteria:
* Contraindication to general anesthesia
* Severe hemostasis and coagulation troubles : Prothrombin level \< 50% and/or platelets level \< 50G/l
* History of duodenal or gastric surgery
* Pregnancy or population of vulnerable patients
* Mental deficiency
* Voluntary withdrawal of informed consent
* Discontinuation by decision of the investigator or the promotor
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02562157
Study Brief:
Protocol Section:
NCT02562157