跳至主要内容
临床试验/CTRI/2025/12/098868
CTRI/2025/12/098868招募中不适用

Safety and Analgesic Effectiveness of the (Femoral Rami and Obturator Nerve Truck) FRONT for Hip Surgery: A Prospective Case Series

AIIMS DELHI1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年12月26日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
20
试验地点
1
主要终点
To assess the analgesic effect of the FRONT block in patients undergoing hip surgery using VAS score till first 24 hours of surgery.

研究概览

简要总结

Over the past decade, regional anesthesia techniques have evolved significantly to better target the sensory innervation of the hip joint while minimizing motor blockade. Among these, the Pericapsular Nerve Group (PENG) block and the Femoral Rami and Obturator Nerve Trunk (FRONT) block have emerged as two distinct strategies aimed at providing effective analgesia for anterior hip procedures. While both blocks share the objective of targeting articular branches innervating the anterior hip .A key theoretical advantage of the FRONT block provides direct and predictable coverage of the obturator nerve, which is a critical contributor to hip joint innervation but is inconsistently reached by the PENG block. Moreover, by clearly defining the fascial planes involved, the FRONT block aims to reduce the variability seen with pericapsular techniques, offering potentially good analgesic effect for hip surgeries .

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Age more than 18 years ASA physical status 1 to 3 Scheduled for elective hip surgery under spinal Able to provide informed consent.

排除标准

  • Allergy to local anesthetics Infection at block site Coagulopathy or on anticoagulant therapy Pre-existing neurological deficits in lower limbs Cognitive impairment or inability to understand pain scoring • Complex hip surgery like revision THR.

结局指标

主要结局

To assess the analgesic effect of the FRONT block in patients undergoing hip surgery using VAS score till first 24 hours of surgery.

时间窗: 0, 2, 4, 6, 12, 24, and 48 hours

次要结局

  • • To evaluate fentanyl consumption postoperatively.(• Time to breakthrough pain in hours)

研究者

发起方
AIIMS DELHI
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Debesh Bhoi

All India Institute Of Medical Sciences, Delhi, India

研究点 (1)

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