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 @ 2:16 PM
Ignite Modification Date:
2025-12-24 @ 2:16 PM
NCT ID:
NCT05513495
Eligibility Criteria:
Inclusion Criteria:
* Doppler measurements must be performed in fetuses with IUGR
* Preterm infants (GA\<37 weeks) with IUGR who were evaluated by Doppler ultrasound were eligible for the study
* These preterm infants must have no enteral nutrition prior to enrolment.
Exclusion Criteria:
* Chromosomal or major congenital abnormalities that may influence the ability to monitor the splanchnic bed (congenital heart defects, abdominal wall defects, or congenital diaphragmatic hernia)
* Inherited metabolic diseases
* Hydrops fetalis
* TORCH infection
* Multiorgan failure
* Infants with spontaneous intestinal perforation
* Infants with skin lesions at the site of sensor placement
* Infants who were hospitalized for shorter than 7 days because of discharge or death
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
1 Minute
Maximum Age:
3 Months
Study:
NCT05513495
Study Brief:
Protocol Section:
NCT05513495