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 @ 2:30 AM
Ignite Modification Date:
2025-12-25 @ 2:30 AM
NCT ID:
NCT01386034
Eligibility Criteria:
Inclusion Criteria:
* Adult between 18 and 75 years
* Patient with short bowel syndrome
* Patient with an incompetent small intestine after intestinal resection
* Patient fed orally and beyond more than 6 weeks after surgery
* Absence of any earlier supplementation with citrulline, glutamine, ornithine a-ketoglutarate, or stimol®
* No current artificial feeding (parenteral)
* No low-sodium diet- No renal, cardiac, respiratory or hepatic insufficiency
* No chronic inflammatory disease (intestinal or other)
* No current corticosteroid treatment
* Fasting blood glucose below 6mmol/L
* Patient able to understand benefits and risks of protocol
* Women who are of childbearing potential must have a negative serum pregnancy test and agree to use a medically acceptable method of contraception throughout the study and for 15 days following the end of the study
* Signed informed consent
Exclusion Criteria:
* Subject not fulfilling inclusion criteria
* Subject mentioned in articles L1121-5 to L1121-8 of "code de la santé publique"
* Pregnancy
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT01386034
Study Brief:
Protocol Section:
NCT01386034