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临床试验/DRKS00000663
DRKS00000663已完成4 期

Investigation of nociceptive and antinociceptivemechanisms under anesthesia using fMRI, EEG and noxious reflexes - fMRT-Nociception

Charité Campus Charité Mitte0 个研究点目标入组 13 人开始时间: 2012年12月17日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
13

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 60 Years(—)
性别
All

入选标准

  • informed consent; age 18-60; no enrollment in other studies under the AMG (German medicinal products law)

排除标准

  • any light or severe illness, especially even at the lightest stage: infections of the respiatory system, muscular diseases, diseases of the cns, chronical pain diseases, drug abuse, medication abuse; claustrophobia; increased risk of aspiration, especially adipositas (BMI > 30 kg/m2); pregnancy and lactation; history or family history of malign hyperthermia; history of family history of severe allergic reactions to propofol, remifentanil, soja, latex; placement in an institution on official order; implants, especially: pace makers, implanted cardioverters, cochlea implants, insulin pumps, nerve stimulators, vascular clips, cava filters, metal splints, screws, wires, plates; extensive or looped tattoos, unremovable piercings, other ferro-magnetic body onaments; unwillingness to comply to the filing and transmission of pseudonymous data about diseases in the scope of the clinical trial; actual of expected future dependence of the study personnell

研究者

发起方
Charité Campus Charité Mitte

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