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临床试验/EUCTR2009-013481-10-NL
EUCTR2009-013481-10-NL进行中(未招募)不适用

Pharmacokinetics of high dose Ropivacaine with and without epinephrine for combined femoral and sciatic nerve block in lower extremity surgery. A pilot study. - RopiPilot

Sint Maartenskliniek0 个研究点开始时间: 2009年8月20日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)

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

  • - Patients = 18 years, = 60 years
  • - Body Weight = 70 kg
  • - ASA classification I – III
  • - Patients undergoing combined femoral and sciatic nerve block for lower extremity orthopaedic surgery
  • - Who will be admitted for at least 48 hours
  • - Written informed consent
  • 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Contra-indications for regional anesthesia (infection at the injection site, coagulopathy)
  • - Known hypersensitivity to amide-type local anesthetics
  • - Known history of peripheral neuropathy
  • - Hepatic or renal insufficiency
  • - Use of fluvoxamine, ciprofloxacin, ketoconazole, erythromycin, clarithromycin, itraconazole, or rifampicin because of their effect on ropivacaine clearance.

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