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 @ 7:08 PM
Ignite Modification Date:
2025-12-24 @ 7:08 PM
NCT ID:
NCT05154357
Eligibility Criteria:
Criteria Inclusion Criteria
* Parent agreeing to take part in the study
* Infant starting oral feeding by the doctor in the neonatal intensive care unit and tolerating it
* Infant born at 26-36+6 gestational week specified according to the last menstruation date of the mother
* Infant being at 32-39+6 postmenstrual week
* Infant having a body weight of 1500 grams and above
* Infant being fed orally once before and tolerating it
* Infant having no health problem except for being a preterm
Exclusion Criteria
* Infant having a gastrointestinal, neurological or genetic illness (such as necrotizing enterocolitis, intracranial bleeding, hydrocephaly, omophalocele, down's syndrome, gastroschisis) and other illnesses
* Infant having no obstacle to oral feeding (such as cleft palate, cleft lip, facial muscle paralysis, craniofacial anomaly)
* Infant being on oxygen support
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
32 Weeks
Maximum Age:
40 Weeks
Study:
NCT05154357
Study Brief:
Protocol Section:
NCT05154357