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 @ 3:37 PM
Ignite Modification Date:
2025-12-24 @ 3:37 PM
NCT ID:
NCT05709392
Eligibility Criteria:
Inclusion Criteria:
Infants born in gestational weeks 30+0-34+6 through vaginal delivery and admitted to neonatal ward in Sweden.
Parents must be able to read Swedish.
Exclusion Criteria:
Infants with known disease when an expanded blood volume is expected will be excluded as early cord clamping is recommended (severe anemia, cardiac disease etc).
Infants with known malformations. Infants with severe or moderate asphyxia (defined as APGAR \< 4 at 5 minutes of age).
Infants where the physician in charge find it inappropriate with delayed cord clamping.
No time for cord clamping has been registered.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
30 Weeks
Maximum Age:
34 Weeks
Study:
NCT05709392
Study Brief:
Protocol Section:
NCT05709392