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临床试验/NCT02186899
NCT02186899Unknown不适用

Comparison of Femoral - Sciatic - Obturator Nerve Block vs General Anesthesia in Combination With Continuous or Bolus Femoral Nerve Block for Arthroscopic ACL Repair Regarding the Time of Patient Mobilasation

Larissa University Hospital1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2014年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
150
试验地点
1
主要终点
Surgery completed without pain for the patient

研究概览

简要总结

Arthroscopic ACL repair can be performed under different types of anesthesia. In the last few years peripheral nerve blocks have increased their popularity for this kind of operation. The investigators want to see how the type of anesthesia and postoperative analgesia effects the time required for patient mobilisation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 - 80 yrs
  • ASA I - III
  • ACL surgery

排除标准

  • Coagulopathy disorders
  • Infection at the puncture site for the interscalene block
  • Neurologic deficit in the arm that is going to be operated
  • Allergy to local anesthetics
  • BMI > 35
  • Psychiatric disorders
  • Patient's refusal
  • Problems with patient communication

研究组 & 干预措施

General Anesthesia Femoral continuous

Active Comparator

General anesthesia plus continuous femoral nerve block

干预措施: General anesthesia femoral continuous (Other)

General anesthesia Femoral bolus

Active Comparator

General anesthesia plus single shot femoral nerve block

干预措施: General Anesthesia femoral bolus (Other)

Femoral Sciatic Obturator Nerve block

Active Comparator

Ultrasound guided femoral plus sciatic plus obturator nerve block

干预措施: Ultrasound Guided Femoral Sciatic Obturator nerve blocks (Other)

结局指标

主要结局

Surgery completed without pain for the patient

时间窗: Completion of the surgery

Use of VAS score

Postoperative pain

时间窗: 1st postoperative day

Use of VAS score

次要结局

  • Mobilization of the knee(24 weeks postoperatively)

研究者

发起方
Larissa University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Marina Simaioforidou

Anesthesiologist

Larissa University Hospital

研究点 (1)

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