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临床试验/NCT05432011
NCT05432011已完成不适用

PENG Block Combined to Lateral Femoral Cutaneous Nerve Block vs. PENG Block Combined to Wound Infiltration for Postoperative Analgesia Following Posterolateral-approached Total Hip Arthroplasty

Campus Bio-Medico University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2022年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
Static Pain Score

研究概览

简要总结

This study aims to analyze the effect of Pericapsular Nerve Group (PENG) Block combined with lateral femoral cutaneous nerve block vs. PENG block combined with wound infiltration for analgesia after elective hip replacement performed with a posters-lateral approach.

Half of participants will receive a PENG Block combined with femoral lateral cutaneous nerve block, while the other half will receive PENG Block combined with wound infiltration

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Elective hip replacement surgery performed with a poster-lateral approach
  • ASA physical status score < 4

排除标准

  • Contraindications to regional anesthesia
  • ASA physical status score ≥ 4
  • Patient's refusal or inability to sign the informed consent
  • Allergies to any drug provided by the study protocol

结局指标

主要结局

Static Pain Score

时间窗: 24 hours

A numerical rating scale (NRS) from 0 (no pain) to 10 (worst imaginable pain) will be used to evaluate pain at rest during 24 hours after surgery

Dynamic Pain Score

时间窗: 24 hours

A numerical rating scale (NRS) from 0 (no pain) to 10 (worst imaginable pain) will be used to evaluate pain on movement during 24 hours after surgery

次要结局

  • Range of hip motion(24 hours)
  • Morphine consumption(6 days)
  • Ability to start physiotherapy during the first postoperative day(24 hours)
  • Quadriceps Strength(24 hours)
  • Ability to ambulate with the help of a walker during the first postoperative day(24 hours)
  • Incidence of block complications(24 hours)
  • Hospital Length of Stay(6 days)

研究者

发起方
Campus Bio-Medico University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Giuseppe Pascarella

Principal Investigator

Campus Bio-Medico University

研究点 (1)

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