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 @ 10:09 PM
Ignite Modification Date:
2025-12-24 @ 10:09 PM
NCT ID:
NCT05651035
Eligibility Criteria:
Inclusion Criteria:
* Gestation week at birth determined according to the mother's last menstrual date is 26-31+6 weeks,
* Postmenstrual week at the time of the study was 32-36+6 weeks,
* Having a body weight of 1500 grams or more at the time of inclusion in the study,
* Suggested by the physician to switch to oral nutrition and switched from enteral nutrition to oral nutrition for the first time,
* Breastfed,
* Preterm infants whose parents' consent was obtained for inclusion in the study and whose parents signed the informed consent form
Exclusion Criteria:
* Receiving oxygen,
* Craniofacial anomalies such as cleft palate, cleft lip, facial muscle paralysis,
* Preterm infants with any gastrointestinal, neurological and genetic disease (necrotizing enterocolitis, third and fourth level intracranial hemorrhage, periventricular leukomalacia, hydrocephalus, down syndrome, omphalocele, non-gastrodeia, short bowel syndrome and other diseases)
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
32 Weeks
Maximum Age:
36 Weeks
Study:
NCT05651035
Study Brief:
Protocol Section:
NCT05651035