NCT05166720CompletedNot Applicable
Clinical Application of the Best Evidence of NIDCAP in Very Low Birth Weight Infants
Children's Hospital of Fudan University1 site in 1 country14 target enrollmentStarted: March 1, 2021Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 14
- Locations
- 1
- Primary Endpoint
- Mean length of stay of VLBWI
Study Overview
Brief Summary
In order to help THE GROWTH and development of VLBWI in Neonatal Intensive Care Unit (NICU) and reduce the interference of external environment to them, we summarized the best evidence of NIDCAP care, and applied the evidence to the intervention group, and observed the compliance of nurses in the intervention group to the application of evidence, and the short-term outcomes of VLBWI.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- — to 1 Day (Child)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Birth weight <1500g;
- •admit within 24 hours of birth;
- •The guardian signs the informed consent;
- •OI (oxygenation index >300)
Exclusion Criteria
- •Newborn with severe congenital malformations or various chromosomal diseases, genetic metabolic diseases, severe neurological diseases;
- •Newborn who did not achieved discharge or death at the end of the study period
Outcomes
Primary Outcomes
Mean length of stay of VLBWI
Time Frame: From the day the VLBWI admitted to the day VLBWI discharged, about two months.
The average length of stay of VLBWI in the intervention group minus the average length of stay of VLBWI in the control group
Secondary Outcomes
- Nurse compliance with NIDCAP evidence content(From the beginning of the NIDCAP intervention to the end of the NIDCAP intervention, about three months.)
Investigators
Study Sites (1)
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