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 @ 2:06 PM
Ignite Modification Date:
2025-12-24 @ 2:06 PM
NCT ID:
NCT05802095
Eligibility Criteria:
Inclusion Criteria:
1. Postmenstrual age 32 and 35 weeks of gestation,
2. Over 1500 g,
3. Switching to oral feeding after feeding with orogastric tube,
4. Who has been breastfed during gavage feeding,
5. Those who have not completed the first 24 hours in the transition from oragastric tube feeding to the oral feeding process,
6. Having cues of readiness for feeding (tolerating enteral nutrition, having a stable oxygen saturation and breathing during feeding, having the ability to lick, swallow and suck, react when mouth and lip are given stimuli),
7. The mother's willingness to breastfeed her baby,
8. Premature babies of parents who volunteered to participate in the study will be included.
Exclusion Criteria:
1. Having diseases other than being premature
2. Able to successfully take the breast in the first attempt,
3. Congenital anomaly,
4. Chromosomal disorders,
5. Having sepsis
6. With intracranial bleeding,
7. Those with a very low birth weight below 1500 g and
8. Less than 32nd gestational week,
9. Premature babies older than 35 weeks of gestation will be excluded.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
32 Weeks
Maximum Age:
35 Weeks
Study:
NCT05802095
Study Brief:
Protocol Section:
NCT05802095