EUCTR2012-003875-20-SE进行中（未招募）1 期
Postoperative pain relief following total hip arthroplasty. A comparison between 3-in-1 blockade (single shot) with ultrasound placement and local infiltration analgesia.
niversitetssjukhuset Örebro0 个研究点开始时间: 2012年12月3日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 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
- •1. 50 - 80 year-old patient undergoing total hip arthroplasty.
- •2. ASA I – III
- •3. Signed and dated Informed Consent.
- •4. The patient is willing and able to comply with the protocol
- •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 0
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •1. Re-operation of a previous total hip arthroplasty.
- •2. Allergy/intolerance to local anaesthetics, Morphine, Adrenaline, Ketorolac or Ropivacaine.
- •3. Serious liver- or renal disease judged by the investigator to be of such dignity as to prevent inclusion into the study.
- •4. Serious heart disease judged by the investigator to be of such dignity as to prevent inclusion into the study,
- •5. Patients with chronic pain who are taking opiate analgesics regularly.
- •6. Major bleeding disorders
- •7. Chronic obstructive pulmonary disease (COPD)
- •8. Severe asthma that is difficult to treat
- •9. Limited breathing capacity due to muscular dystrophy
- •10. Sleep apnoea syndrome
- •11. Other contraindication to spinal anaesthesia such as spinal stenosis, local infection or contraindications to local anaesthetics.
- •12. Participation in another clinical medicinal trial during the last 30 days or where follow-up is not completed.
研究者
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