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临床试验/NCT03031431
NCT03031431已完成不适用

Electricity-free Infant Warmer for Newborn Thermoregulation in Rwanda

Boston Children's Hospital1 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2016年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
130
试验地点
1
主要终点
Temperature/Effectiveness

研究概览

简要总结

Hypothermia contributes to a significant portion of neonatal deaths. Kangaroo mother care (KMC) is a safe and effective method of warming; however, it is not always feasible, and not possible in settings such as resuscitation or clinical instability. Electric warmers are the standard of care in developed countries, but are extremely costly, complicated with risk of causing both hypo and hyperthermia with misuse, and often not feasible in settings without stable electricity. Through a multi-institutional collaboration, the investigators have developed an electricity-free infant warmer. After laboratory based prototype testing for safety and efficacy, the investigators aim to study the supervised use of the warmer under routine implementation conditions in a resource-limited setting.

详细描述

Hypothermia contributes to a significant portion of neonatal deaths. Kangaroo mother care (KMC) is a safe and effective method of warming; however, it is not always feasible, and not possible in settings such as resuscitation or clinical instability. Electric warmers are the standard of care in developed countries, but are extremely costly, complicated with risk of causing both hypo and hyperthermia with misuse, and often not feasible in settings without stable electricity. Through a multi-institutional collaboration, the investigators have developed an electricity-free infant warmer. After laboratory based prototype testing for safety and efficacy, the investigators aim to study the supervised use of the warmer under routine implementation conditions in a resource-limited setting. The primary aim of Phase 1 is to determine if the infant warmer is a safe, effective, usable and functional addition to KMC. This is planned in a convenience sample of patients in two district hospitals, one in a relatively warm environment, and one in a colder setting using quantitative methods and observer audits of usability and functionality. After determination of safety and effectiveness and making any necessary modifications to the warmer, Phase 2 aims to study the warmer in rural health centers and transport, as this is where we ultimately aim to use the electricity free devices due to the limited access to functioning and stable electricity in these settings. The overall goal of the project is dissemination of the study results, and ultimately the infant warmer to the district and national level for key policy makers and stakeholders, as well as globally via publication.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
— 至 3 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Any infant with the following criteria for whom caregiver is not available for Kangaroo Mother Care, or Kangaroo Mother Care is not adequate (less than ½ degree Celsius per hour rise in temperature).
  • axillary temperature < 36 degrees C and ≥35 degrees C 1a) If an electric warmer is available and the infant's temperature is < 35 degrees C, then the infant would start by being warmed on the electric warmer until the infant's temperature reaches 36 degrees C, then can start non-electric infant warmer use
  • Infants at-risk for hypothermia (criteria: estimated post-menstrual age of < 35 weeks or current body weight of < 2.5 kg)

排除标准

  • Any infant whose family is unwilling to consent to study.
  • Mothers who are critically ill at the time of infant eligibility or deemed not medically stable by nursing staff to be approached for consent.
  • Any infant with a contraindication to Kangaroo Mother Care (medical instability) and electrical heating source available.
  • Any infant with initial temperature < 35 degrees C and electrical heating source available.
  • Infants within the first hour of admission to neonatal unit or first hour of life in maternity.
  • Infants requiring phototherapy
  • Infants with significant skin condition
  • Infants with Hypoxic Ischemic Encephalopathy (HIE)
  • Stopping Criteria:
  • If an electric heating source is available, the infant will be taken off the study and warmed with an appropriate source of electric heat if the infant:
  • Is hypothermic and temperature decreases on any measurement
  • Is hypothermic and temperature does not begin to rise within 30 minutes
  • Is hypothermic and not heating at a rate of > ½ degree C per hour until temperature is >36.5 degrees C
  • Has a temperature that falls below 36 degrees C despite maximum exposure to the heat source
  • Is ever considered to be too severely ill by the medical team to be safely cared for in the non-electric infant warmer.
  • The warmer will be removed once its temperature drops below 36 degrees, and/or the phase change material begins to harden.

结局指标

主要结局

Temperature/Effectiveness

时间窗: Up to 6 months

The infant warmer will be evaluated on the number of time is able to successfully achieve and maintain a normal body temperature for patients who are hypothermic and those patients at risk of hypothermia because of a \< 2.5 kg birth weight or \< 35 week gestational age.

次要结局

  • Usability(Up to 6 months)
  • Functionality(Up to 6 months)
  • Qualitative Survey(Up to 1 year)

研究者

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

Anne Hansen

MD

Boston Children's Hospital

研究点 (1)

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