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:
2025-12-25 @ 12:32 AM
Ignite Modification Date:
2025-12-25 @ 12:32 AM
NCT ID:
NCT02292667
Eligibility Criteria:
Inclusion Criteria:
* ASA (American Society of Anesthesiologists) physical status 1, 2 or 3
* Elective surgery for open repair of an aortic abdominal aneurysm performed in the Vascular Surgery Unit of the University Hospital of Besancon
* Informed consent given
* Health medical insurance affiliation
Exclusion Criteria:
* Poor adherence to protocol attended
* Incapacity to consent
* Pregnancy and/or breast feeding
* Endovascular repair of aortic abdominal aneurysm
* Emergent surgery of a rupture or a fissuration of aortic abdominal aneurysm
* Chronic medical treatment by clopidogrel if clopidogrel not stopped 5 days before surgery at least
* Chronic medical treatment by prasugrel if prasugrel not stopped 7 days before surgery at least
* Chronic medical treatment by ticlopidine, inhibitors of phosphodiesterase , inhibitors of glycoprotein IIb/IIIa, adenosine triphosphate analogs or thrombin receptor antagonists
* Congenital or acquired bleeding disorder
* Incapacity to use patient-controlled analgesia device
* Chronic opioid abuse or dependence
* Chronic renal failure defined as a clearance \< 30 ml/min
* Severe hepatic failure
* Other contraindications to ropivacaïne (allergy, medical history of porphyria, hypovolemia)
* Contraindications to acetaminophen
* Contraindications to morphine
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02292667
Study Brief:
Protocol Section:
NCT02292667