跳至主要内容
临床试验/NCT05320913
NCT05320913Unknown不适用

Pericapsular Nerve Group (PENG) Block Combined With Periarticular Multimodal Drug Injection (PMDI) Versus Isolated PMDI for Pain Management After Total Hip Arthroplasty: a Randomized Controlled Trial

Yonsei University1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2022年4月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
58
试验地点
1
主要终点
Numeric rating scale pain score

研究概览

简要总结

Adequate pain control after total hip arthroplasty is crucial for early ambulation and patient satisfaction. However, there is no consensus about optimal pain control after post operation. In general, the periarticular multimodal durg injection block has been done for pain control in primary total hip arthroplasty. The pericapsular nerve group (PENG) block has been recently introduced a new technique for blockade of the articular branches of the femoral, obturator and accessory obturator nerves. PENG block is possible to provide sufficient analgesia and preserve lower limb muscle strength. The investigators will compare PENG and PMDI block with isolated PMDI block in patients undergoing total hip arthroplasty.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •1. Patients aged 19 years old or older, with American Society of Anesthesiologists Physical Status 1-3, and scheduled for elective unilateral total hip arthroplasty

排除标准

  • •Allergy or intolerance to any of the drugs used in the study
  • •Hepatic or renal insufficiency
  • •Opioid dependency
  • •Coagulopathy
  • •Pre-existing neurologic or anatomic deficits in the lower extremities
  • •Severe psychiatric illness

研究组 & 干预措施

Pericapsular nerve group(PENG) block combined with periarticular multimodal drug injection (PMDI)

Experimental

Participants receiving pericapsular nerve group(PENG) block combined with periarticular multimodal drug injection (PMDI)

干预措施: Pericapsular nerve group(PENG) block combined with periarticular multimodal drug injection (PMDI) (Procedure)

isolated periarticular multimodal drug injection (PMDI)

Active Comparator

Arm Description: Participants receiving isolated periarticular multimodal drug injection (PMDI)

干预措施: isolated periarticular multimodal drug injection (PMDI) (Procedure)

结局指标

主要结局

Numeric rating scale pain score

时间窗: at 24 hours postoperatively

Pain intensity at rest evaluated by an 11-point numeric rating scale (NRS: 0 = no pain, 10 = worst imaginable pain) at 24 hours postoperatively

次要结局

  • Pain score measured at 6 hours postoperatively and 48 hours postoperatively(Pain score measured at 6 hours postoperatively and 48 hours postoperatively)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验