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 @ 1:41 PM
Ignite Modification Date:
2025-12-24 @ 1:41 PM
NCT ID:
NCT05097495
Eligibility Criteria:
Inclusion Criteria:
* The preterm infants whose parents agree to participate in the research and sign the informed consent form;
* Who have no congenital anomaly;
* Who have no chronic disease;
* Who have undergone no surgical procedure;
* Who have no neurological symptoms;
* Who have no NEC (necrotizing enterocolitis) diagnosis;
* Who are not sedated;
* Who are not hypoglycemic;
* Who have been administered no pharmacological analgesic method 4 hours before;
* Who are born between ≥28 and ≤36+6 gestation weeks, or are in between ≥28 and ≤36+6 gestation weeks during the procedure.
Exclusion Criteria:
* The infants whose parents do not agree to participate in the research and do not sign the informed consent form;
* Who have a congenital anomaly;
* Who have a chronic disease;
* Who had undergone a surgical procedure;
* Who have neurological symptoms;
* Who have NEC (necrotizing enterocolitis) diagnosis;
* Who are sedated;
* Who are hypoglycemic;
* Who have been administered no pharmacological analgesic method 4 hours prior;
* Who were between \<28 and \>36+6 gestation weeks.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
1 Day
Maximum Age:
28 Days
Study:
NCT05097495
Study Brief:
Protocol Section:
NCT05097495