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临床试验/ISRCTN13554391
ISRCTN13554391已完成不适用

Pulsatile, audible, tactile stimulation for premature infants in neonatal intensive care units to reduce pain and increase weight gain

Sociedad Peruana de Pediatría0 个研究点目标入组 120 人开始时间: 2015年9月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Medically stable
  • 2. Gestational age between 30 and 33 weeks + 6 days
  • 3. Birth weight between 1000 and 1400 grams
  • 4. Weight at the time of recruitment > 1000 grams
  • 5. Parental informed consent

排除标准

  • 1. APGAR score < 7 at 5 minutes.
  • 2. Genetic abnormalities, gastrointestinal and cardiac birth defects, central nervous system birth defects, intrauterine growth retardation.
  • 3. Diseases related to prematurity including: severe hyperbilirubinemia, grade III or IV intraventricular hemorrhage, necrotising enterocolitis, chronic lung disease.
  • 4. Persistent infections or metabolic problems during hospitalization.
  • 5. Maternal history of: alcohol or illicit drugs exposure, syphilis , hepatitis B , HIV and
  • other intrauterine infections .
  • 6. Medical conditions that alter the body movement or the ability to participate in the
  • intervention, pathological fractures, bone deformities or seizures.
  • 7. Outgoing or scheduled surgery within the first 28 days of life.
  • 8. Use of sedatives or painkillers at the onset of the study or in the previous 72 hours.
  • 9. Use of postnatal steroids.

研究者

发起方
Sociedad Peruana de Pediatría

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