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:
2025-12-25 @ 3:46 AM
Ignite Modification Date:
2025-12-25 @ 3:46 AM
NCT ID:
NCT04528602
Eligibility Criteria:
Inclusion Criteria:
* The preterm infants whose
* Parents have agreed to participate in the study and have signed the informed consent form,
* Who have no congenital anomalies,
* Have no chronic illnesses,
* Have undergone Underwent no surgical procedures,
* Have no neurological symptoms,
* Have not been diagnosed with sepsis,
* Have not been sedated,
* Have not received any pharmacological analgesic method four hours before,
* Have been born between ≥28 and ≤36+6 gestational weeks or have been born earlier and are between ≥28 and ≤36+6 gestational weeks during the application, will be included.
Exclusion Criteria:
The preterm infants whose
* Parents have not agreed to participate in the study and have not signed the informed consent form,
* Who have congenital anomalies,
* Have chronic illnesses,
* Have undergone surgical procedures,
* Have neurological symptoms,
* Have been diagnosed with sepsis,
* Have been sedated,
* Have received pharmacological analgesic methods four hours before,
* Were between \<28 and \>36+6 gestational weeks, will be excluded.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
1 Day
Maximum Age:
28 Days
Study:
NCT04528602
Study Brief:
Protocol Section:
NCT04528602