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临床试验/NCT06582667
NCT06582667尚未招募不适用

Assessing the Effectiveness and Safety of Pericapsular Nerve Group (PENG) Block in Hip Fracture Patients on Antithrombotic Therapy: A Randomized Controlled Trial

Alexandria University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年9月17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
入组人数
100
试验地点
1
主要终点
Bloody Tab on the Needle:

研究概览

简要总结

PENG block will be done on patients with hip fracture either receiving antithrombotic therapy or not under ultrasound guidance

详细描述

Patients will be randomized into two groups:

Group A (Antithrombotic Therapy Group): 50 Patients on continuous antithrombotic therapy will receive BENG block.

Group C (Control Group): 50 Patients without antithrombotic therapy will receive BENG block.

Intervention:

PENG Block: Standardized administration of the PENG block will be performed by experienced anesthesiologists for both groups using ultrasound device.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Double (Participant, Outcomes Assessor)

盲法说明

outcomes assessor

入排标准

年龄范围
65 Years 至 85 Years(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age 65 years or older
  • •diagnosis of hip fracture
  • •scheduled for surgical intervention within 48 hours
  • •Informed consent obtained.

排除标准

  • •Allergy to local anesthetics,
  • •Contraindications to the PENG block
  • •inability to provide informed consent.

研究组 & 干预措施

group A: PENG block in hip fracture with antithrombotic therapy

Experimental

50 patients will receive US guided PENG block and on antithrombotic therapy in hip fracture

干预措施: PENG block (Procedure)

group C: PENG block in hip fracture without antithrombotic therapy

Experimental

50 patients will receive US guided PENG block without antithrombotic therapy in hip fracture

干预措施: PENG block (Procedure)

结局指标

主要结局

Bloody Tab on the Needle:

时间窗: immediately during the procedure ( first 10 minutes after PENG block)

Presence of blood on the needle during the performance of the PENG block.

Incidence of Hematoma Formation

时间窗: first 48 hours postintervention

The occurrence and severity of hematomas at the PENG block site. Measurement: Regular clinical examinations and imaging studies to assess for hematoma formation.

Rest and mobilization pain by numerical rating scale

时间窗: 1 hour and 6 hours after surgery, on the same day of surgery (D 0) and first day postoperative(D 1) at 8 a.m., 1 p.m. and 6 p.m.

post intervention to be assessed 0-10

次要结局

  • Postoperative quadriceps strength(first day postoperative postoperative (12 hours after surgery))
  • length of hospital stay in days(from the date of admission to the date of discharge)
  • The quality of Postoperative functional recovery and the variations and differences between groups will be assessed using the validated arabic version of the quality-of-recovery 15-items score (QoR-15)(On the same day of surgery ( 12 hours after surgery) and first day postoperative)
  • Incidence of Nerve Injury(after performing the block ( 12 hours after surgery) and subsequent assessments on the next 48 hours)
  • - Perioperative opiate use(from the end of surgery to 48 hours postoperative)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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