Neonatal Adaptation Clinical Trial
Official title:
Features and Differences Between Neonates Undergoing Body Bag With Polyethylene and Conventional Drying During Neonatal Adaptation in Maternal and Child Headquarters Hospital and the Victoria Hospital Engativá, Bogotá, 2013
INTRODUCTION: Hypothermia in the newborn causes morbid conditions. In developing countries
in the basic technology for neonatal adaptation may not be available. Polyethylene bags may
be an alternative to lamp radiant heat to prevent hypothermia OBJECTIVE: To characterize the
differences between babies undergoing body bag with polyethylene or conventional drying
during neonatal adaptation in the Hospital de la Victoria and Hospital de Engativá, Bogotá,
Colombia, 2013.
MATERIALS AND METHODS: parallel-group randomized controlled trial. Groups: dried
conventional (control) or polyethylene body bag (intervention). The procedure lasted 10
minutes, the bag body and / or radiant heat lamp was removed. Environment temperature and
humidity, temperature in the body segments 1-5-10-60-120 minutes and APGAR was measured.
Statistical Analysis: Descriptive bivariate statistical inference and calculated. Risk ratio
(RR) and confidence intervals (CIs) were determined using contingency tables for risk
analysis of the outcome. The study was approved by the hospital ethics committee of victory.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04594824 -
Defining Reference Ranges for Cerebral Oxygenation In Neonates (COIN) During Immediate Neonatal Transition After Birth
|