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临床试验/IRCT2017080935601N1
IRCT2017080935601N1已完成3 期

Comparative evaluation of the effect of propofol_ketamine and propofol_remifentanil for deep sedation and analgesia during painful procedures in 6 month to 14 year old children with acute lymphoblastic leukemia

Isfahan University of Medical Sciences0 个研究点目标入组 81 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
81

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
6 months 至 14 years(—)
性别
All

入选标准

  • The inclusion criteria were included, Children aged between Six months to fourteen years old with Hematologic Malignancies (such as acute lymphocytic leukemia) were candidates for painful intervention Lumbar Puncture; Bone marrow aspiration/Biopsy. Non-entry criteria include patients with head trauma; High intraocular pressure (IOP); or High intracranial pressure (ICP); cardiovascular or repertory or liver diseases; epilepsy or history of seizure; Neurological disorder ;tumor or metastasis of the brain; usage of analgesic or sedative drugs in before intervention; chronic pain syndrome; and not having to participate in the study; history of allergy or allergic reaction to Our study drugs Excluded criteria include any complications during intervention that causes the anesthetic program to change

排除标准

  • 未提供

研究者

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