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临床试验/ITMCTR2026001700
ITMCTR2026001700进行中(未招募)4 期

Dexmedtomidine Versus Midazolam for Sedation in Mechanically Ventilated Neonates: A Comparative Study

University of Baghdad0 个研究点开始时间: 2025年6月25日最近更新:
适应症

试验速览

阶段
4 期
状态
进行中(未招募)

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

年龄范围
28 至 36(—)
性别
All

入选标准

  • Neonates were eligible for inclusion if they met all of the following criteria: (a) gestational age between 28 and 36 weeks at birth; (b) admission to the NICU awith a clinical indication for invasive mechanical ventilation; (c) anticipated duration of mechanical ventilation of at least 24 hours; and (d) informed verbal consent obtained from a parent or legal guardian.

排除标准

  • Neonates were excluded if any of the following conditions were present: (a) major congenital anomalies, including significant cardiac malformations, neurological abnormalities, or syndromic conditions; (b) severe hemodynamic instability requiring high-dose inotropic or vasopressor support (defined as the need for more than one vasoactive agent or a single agent at a dose exceeding standard thresholds); (c) known or suspected hypersensitivity to dexmedetomidine or midazolam; (d) preexisting renal or hepatic impairment that could significantly alter drug metabolism or clearance.

研究者

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