跳至主要内容
临床试验/NCT00904228
NCT00904228已完成不适用

Effectiveness of Plastic Lined Hats for Prevention of Hypothermia in Premature Newborns in the Delivery Room

University of Texas Southwestern Medical Center2 个研究点 分布在 1 个国家目标入组 260 人开始时间: 2008年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
260
试验地点
2
主要终点
Hypothermia

研究概览

简要总结

The purpose of this research project is to ascertain the effectiveness of plastic head covering in prevention of hypothermia. Hypothermia is defined by body temperature <36.5º Celsius by the World Health Organization. The surface area of the head is about 20% of total body surface of a newborn infant and is a major source of heat loss. The objective is to compare rectal temperature upon admission to the neonatal intensive care between preterm neonates who had stockinet head covering and those who had plastic-lined stockinet head covering placed in the delivery room. The investigators aim to demonstrate that plastic-lined head covering is more effective than stockinet head covering alone in maintaining body temperature.

详细描述

A prospective randomized control trial will be conducted in Parkland Memorial Hospital (PMH) neonatal intensive care unit (NICU) Dallas, Texas. Consent will not be obtained since: placement of plastic and/or stockinet head covering on the neonate is part of routine resuscitation care at PMH and by Neonatal Resuscitation Program (NRP) minimal risk to the preterm neonate is involved, post-delivery consent will be of little value since intervention only last ~24minutes, and obtaining informed consent from a mother who has labor pains or is on pain medication may be difficult.

Randomization of the neonates will be carried out in the delivery room by opening a sealed, opaque envelope just prior to birth. Qualified preterm newborns will be stratified into 2 OB EGA groups: (≤28weeks obstetrical(OB)estimated gestational age (EGA) and 29-32weeks OB EGA. In each stratified group, the newborns will be further randomized to control arm (stockinet head covering) or the intervention arm (plastic-lined head covering). Each arm of the study will have a sample size of 65, allowing for 130 infants in each OB EGA stratified group and for a sample size total of 260. Treatment versus control will be assigned by blocks of 8 by using a random permutation table. The assignment will be sealed in an opaque envelope by a non-participant person of the research.

The PMH high-risk resuscitation (RESUS) team attends all deliveries of infants ≤32 weeks OB EGA. The RESUS team is comprised of a resuscitation nurse, a respiratory therapist, and a practitioner. Neonatology fellow and/or attending may also attend these deliveries.

The use of warming aids by the RESUS team is standardized in the following manner: Randomization envelope will be opened. All infants will be taken from the obstetrician by the practitioner to an Ohio radiant warmer that has been pre-warmed to 100% capacity prior to the delivery of the infant. A food-grade storage (polyethylene) bag (will be referred as "poncho") will be used on all infants with the EGA of 32 weeks or less OB EGA to decrease evaporative and convective heat loss. The poncho will be placed by cutting a hole at the closed end of the bag for the purposes of inserting the head through it. The infants will not be dried except for the face as recommended by NRP. All infants that are ≤28weeks OB EGA will have a transwarmer mattress gel pad activated and placed on the radiant warmer during resuscitation and during transport as per PMH NICU and NRP standard practice. The appropriate head covering will then be placed to the level of the forehead on the infant as per randomization assignment. If access to the infant's umbilical cord is needed, a hole will be cut at the appropriate location. All infants will be transported in a dedicated isolette for resuscitation that has been prewarmed to 38ºC. The warming aids will be in place until the infant's arrival in the NICU.

The RESUS team will gather the following data in the delivery room: environmental temperature of the delivery room, rectal temperature immediately after delivery, annotation of warming aids implemented. The RESUS team also cares for the infant in the first 4 hours of life. Initial vital signs (heart rate, respiratory rate, and blood pressure), temperature, need of ventilation, need of intervention will be recorded by the RESUS team. After 4 hours the care will be assumed by the primary NICU team as per our standard practice.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
— 至 1 Hour(Child)
性别
All
接受健康志愿者

入选标准

  • Infants with less than 33 week gestational age by obstetrical dating
  • Infants delivered in Parkland Memorial Hospital Labor and Delivery areas
  • Infant whose delivery was attended by the Parkland Neonatal Resuscitation Team
  • Infant whos is viable

排除标准

  • Infant who has 33 week gestational age or greater by obstetrical dating
  • Infant who is deemed non-viable
  • Infant who did not have the Parkland Neonatal Resuscitation Team present at time of birth
  • Infant with congenital anomaly which precludes measurement of rectal temperature (such as anal atresia or imperforate anus)

研究组 & 干预措施

Plastic Cap

Experimental

Plastic lined stockinet cap (polyethylene bag)

干预措施: placement of plastic cap during delivery room stabilization (Other)

Stockinet Cap

Active Comparator

Usual practice

干预措施: placement of routine cap during delivery room stabilization (Other)

结局指标

主要结局

Hypothermia

时间窗: 1 hour

admission rectal temperature \<36.5C

次要结局

  • Mortality(1 year)
  • Infection(1 year)
  • Necrotizing enterocolitis(1 year)
  • Intraventricular Hemorrhage(1 year)
  • Bronchopulmonary Dysplasia(1 year)
  • Days on Ventilator(1 year)
  • Length of hospital stay(1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Myra Wyckoff

Professor of Pediatrics

University of Texas Southwestern Medical Center

研究点 (2)

Loading locations...

相似试验