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Clinical Trials in Turkey / NCT06672913
Recruiting Not applicable

Impact of Standardized Skin-to-Skin Care on Clinical Outcomes in Infants Born ≤ 32 Weeks: A Multicenter Study

NCT06672913 · tracked via the Priya Life Science Turkey tracker
Sponsor
Baskent University Ankara Hospital
Phase
Not applicable
Started
2024-09-01
Last updated
2024-11-04

Condition(s) studied

PrematureSkin to Skin ContactBreast FeedingNecrotizing EnterocolitisRetinopathy of Prematurity

Investigational drug(s) / intervention(s)

skin to skin contact care

skin to skin contact care: Early and regular skin to skin contact in NICU GA: \< 28 weeks: After the 72nd hour GA: 28 - 32 weeks: As soon as stabilization is ensured

Study summary

This study is a multi-center, prospective pre-post clinical study conducted under the leadership of the Turkish Neonatal Society. It aims to investigate the effects of a standardized skin-to-skin care in NICU, initiated early and applied regularly, on recieving exclusive mothers' milk at discharge and clinical outcomes for preterm infants born ≤ 32 weeks of gestation.

1. Primary Objective: To evaluate the rate of receiving exclusive mothers' milk at discharge for infants born ≤ 32 weeks of gestation who have received skin-to-skin care in accordance with the study protocol.
2. Secondary Objective: To evaluate the rates of neonatal sepsis, intraventricular hemorrhage, and necrotizing enterocolitis (stage 2 and above) as well as the length of hospital stay for infants born at or below 32 weeks of gestation who have received skin-to-skin care in accordance with the study protocol.

Eligibility

Sex
ALL
Min age
1 Day
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Infants born at gestational age ≤ 32 weeks Exclusion Criteria: * Death before NICU discharge * Abdominal wall defects

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Baskent University Ankara Turkey (Türkiye) Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06672913 on ClinicalTrials.gov ↗ ← All trials in Turkey