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 @ 5:56 PM
Ignite Modification Date:
2025-12-24 @ 5:56 PM
NCT ID:
NCT07275268
Eligibility Criteria:
Inclusion Criteria:
Premature under 37 weeks of amenorrhea with an adverse event of special interest such as :
* altered abdomen with bloating or presence of previsouly unknow marked collateral circulation,
* absence of spontaneous transit (\> 48 hours),
* episode of rectal bleeding,
* repeated regurgitation/vomiting (during more than 50% of feedings),
* prolonged fasting (\>12 hours), OR
* increase in cardiorespiratory events on continuous monitoring associated with one of the elements listed above.
Exclusion Criteria:
* organic malformation detected during prenatal monitoring or discovered in the immediate postnatal period,
* chromosomal abnormality detected during prenatal monitoring or discovered in the immediate postnatal period,- spontaneous perforation occurring during the first week of life.
Healthy Volunteers:
False
Sex:
ALL
Maximum Age:
36 Weeks
Study:
NCT07275268
Study Brief:
Protocol Section:
NCT07275268