Eligibility Module

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 @ 10:00 PM
Ignite Modification Date: 2025-12-24 @ 10:00 PM
NCT ID: NCT06628232
Eligibility Criteria: Inclusion Criteria: * Mother 18 years of age or older * Mother is literate * Whether the mother gives birth naturally or by caesarean section * Uncomplicated pregnancy and birth history in mother * Mother\'s voluntary participation in the study * Preterm babies between 34 0/7-36 6/7 weeks * Prematurity at 34 0/7-36 6/7 weeks and weight appropriate for the week (Appropriate Gestational Age- AGA), * The baby should be fed at least 1 hour in advance. * It has been 1 hour since the last painful intervention on the baby. * 6Heel blood should be taken 6 hours after taking analgesic, sedative and anticonvulsant medications. Exclusion Criteria: * The baby has a fever * The baby receiving oxygen therapy, * The baby receiving antibiotic treatment * The baby has a congenital anomaly * The baby having the bed side and heater underneath * The baby receiving phototherapy, * The baby is connected to a mechanical ventilator * Babies whose blood was not collected on the first attempt
Healthy Volunteers: True
Sex: ALL
Minimum Age: 34 Weeks
Maximum Age: 36 Weeks
Study: NCT06628232
Study Brief:
Protocol Section: NCT06628232