EUCTR2016-000082-23-NL进行中（未招募）不适用
Median Local Anaesthetic Dose (MLAD) of intrathecal Bupivacaine in total knee arthroplasty
Reinier de Graaf Groep0 个研究点开始时间: 2016年2月15日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- •- ASA I, II or III
- •- 18 years or older
- •- primary total knee arthroplasty
- •- willing to participate
- •- sufficient command of Dutch
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 15
排除标准
- •A potential subject who meets any of the following criteria will be excluded from participation in this study:
- •- Hypersensitivity to local anaesthetics or any of the other excipients of Bupivacaine
- •- Any other contraindications relate to intrathecal anaesthesia
- •- CNS disease, e.g. menigitis, tumor, poliomyelitis, cerebral haemorrhage
- •- Spinal stenosis and diseases or recent trauma to the cervical column
- •- Pernicious anemia with symptoms related to cervical degradation
- •- Pyogenic infections of the skin close to the injection site
- •- Cardiogenic or hypovolemic shock
- •- Disturbance in coagulation or treatment with anti-coagulants
- •- Patient is participating in a medicinal study
- •- Noncompliant with intrathecal anaesthesia
- •- No Local Infiltration Anaesthesia (LIA) possible
- •- Patients who are incompetent to decide
研究者
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