跳至主要内容
临床试验/NCT07003633
NCT07003633尚未招募不适用

Preoperative Analgesia: The Effect of the Pericapsular Nerve Group (PENG) Block Administered Preoperatively in Patients With Hip Fractures on Preoperative Analgesic Efficacy, Early Postoperative Discharge, Mortality, and Morbidity.

Sakarya University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Preoperative Pain Scores and Opioid Consumption

研究概览

简要总结

The aim is to provide effective preoperative analgesia in patients undergoing surgical procedures due to hip fractures by administering a pericapsular nerve group (PENG) block under ultrasound guidance. This approach seeks to increase patient satisfaction, reduce analgesic requirements, enable earlier discharge, and decrease morbidity and mortality.

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
Single (Participant)

盲法说明

The patients will be randomized to their rescpective groups with closed envelope method.

入排标准

年龄范围
45 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients undergoing hip farcture surgery

排除标准

  • •Chronic analgesics consumption
  • •Patients contraindicated for neuraxial anesthesia
  • •Alcohol and drug addiction
  • •Allergies to local anesthetics and opioids
  • •Patients who refuses to participate in the study

研究组 & 干预措施

Group PENG

Experimental

Group PENG will involve the patients who will be performed PENG block 24 hours before surgery.

干预措施: PENG block with 0.25% bupivacaine guided by ultrasound. (Procedure)

Group Control

No Intervention

Group Control will involve the patients who will not be performed PENG block preoperatively.

结局指标

主要结局

Preoperative Pain Scores and Opioid Consumption

时间窗: 24 hours preoperatively

Preoperative pain of patients will be assessed with NRS (Numeric Raitng Scale) which ranges from 0 (no pain) to 10 (the most severe pain imaginable).

次要结局

  • Opioid Consumption(24 hours preoperatively)
  • Discharge Time(From surgery to discharge up to 30 days)
  • Postoperative Mortality and Morbidity(30 days after surgery)

研究者

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

Alim Miniksar, MD

Anesthesiology and Reanimation Resident, M.D.

Sakarya University

研究点 (1)

Loading locations...

相似试验