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临床试验/NCT02271555
NCT02271555Unknown4 期

Inonu University, Turgut Ozal Medical Center, Department of Anesthesiology and Reanimation Malatya

Inonu University1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2014年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
58
试验地点
1
主要终点
The effects of remifentanil on the heart rate after electroconvulsive therapy

研究概览

简要总结

The investigators will be evaluated the effects of a single loading dose of remifentanil (1µg/kg), administered as an adjunct to sevoflurane, on duration of hemodynamic profile, seizure activity, and recovery times during electroconvulsive therapy (ECT) in patients with major depression

详细描述

Major depressive patients will enrolled this trial. Mean arterial pressure (MAP) and heart rate (HR) and peripheral oxygen saturation values will be recorded prior to anesthetic induction (T1); following anesthetic induction (T2); and 0, 1, 3, and 10 minute after the seizure have ended (T3, T4, T5, and T6, respectively). The peak heart rate during the seizure will be recorded from the Electrocardiogram.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Major depressive patients

排除标准

  • younger than 18 years, pregnant, had a history of myocardial infarction in the previous six months, atrial fibrillation or flutter, heart block, unregulated hypertension, cerebrovascular diseases, known drug allergy.

研究组 & 干预措施

sevoflurane-remifentanil (Group SR)

Active Comparator

Sevoflurane will be initiated, at 8% for anesthesia induction until loss of consciousness will achieve, at which point it will be discontinued. After the loss of consciousness remifentanil will be administered to Group sevoflurane-remifentanil in the form of a 1 µg/kg intravenous bolus.

干预措施: Sevoflurane (Drug)

sevoflurane-remifentanil (Group SR)

Active Comparator

Sevoflurane will be initiated, at 8% for anesthesia induction until loss of consciousness will achieve, at which point it will be discontinued. After the loss of consciousness remifentanil will be administered to Group sevoflurane-remifentanil in the form of a 1 µg/kg intravenous bolus.

干预措施: Remifentanil (Drug)

sevoflurane-saline (Group SS)

Placebo Comparator

Sevoflurane will be initiated, at 8% for anesthesia induction until loss of consciousness will achieve, at which point it will be discontinued. Placebo is 0.9% saline. After the loss of consciousness saline will be administered to Group sevoflurane-saline in the form of intravenous bolus.

干预措施: Sevoflurane (Drug)

sevoflurane-saline (Group SS)

Placebo Comparator

Sevoflurane will be initiated, at 8% for anesthesia induction until loss of consciousness will achieve, at which point it will be discontinued. Placebo is 0.9% saline. After the loss of consciousness saline will be administered to Group sevoflurane-saline in the form of intravenous bolus.

干预措施: Saline (Drug)

结局指标

主要结局

The effects of remifentanil on the heart rate after electroconvulsive therapy

时间窗: 20 minute

Prior to anesthetic induction (T1); following anesthetic induction (T2); and 0, 1, 3, and 10 minute after the seizure have ended (T3, T4, T5, and T6, respectively).

次要结局

  • Seizure duration(20 minute)
  • The effects of remifentanil on the mean arterial pressure after electroconvulsive therapy(20 minute)

研究者

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

Feray Erdil

Associated professor

Inonu University

研究点 (1)

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