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 @ 3:18 AM
Ignite Modification Date:
2025-12-25 @ 3:18 AM
NCT ID:
NCT04250805
Eligibility Criteria:
Inclusion criteria :
* Major patient;
* Having an indication for placement of PRG (percutaneous radiological gastrostomy);
* Patient hospitalized for a minimum of 24 hours post gastrostomy;
Non-inclusion criteria :
* Pregnant or lactating woman;
* Legal incapacity or limited legal capacity. Medical or psychological conditions which do not allow the subject to understand the study and sign the consent (art. L.1121-6, L.1121-7, L.1211-8, L.1211-9);
* Not knowing how to read and / or write French;
* Allergy and / or known hypersensitivity to lidocaine and / or ropivacaine or to other local anesthetics with amide bond or to one of the excipients;
* Recurrent porphyrias (genetic, hereditary diseases affecting the production of hemoglobin);
* Patient on beta blockers during the installation of PRG (Percutaneous Radiological Gastrostomy);
* Indication of gastrostomy button placement.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04250805
Study Brief:
Protocol Section:
NCT04250805