NL-OMON43572已完成4 期
Median Local Anaesthetic dose (MLAD) of Intrathecal Bupivacaine in anterior supine intermuscular total hip arthroplasty - ED50 of Intrathecal Bupivacaine in Total Hip Arthroplasty
Reinier de Graaf Groep0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 25
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
- 18 至 99(—)
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 to III
- •- 18y or older
- •- Primary uncemented THA-ASI
- •- Willing to participate
- •- Speaking Dutch language
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 anesthetics or any of the other excipients of Bupivacaine
- •- Any other contraindications relate to intrathecal anesthesia
- •- CNS disease, e.g. meningitis, 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 to intrathecal anesthsia
- •- Patients who are incompetent to decide
研究者
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