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临床试验/CTRI/2023/10/058655
CTRI/2023/10/058655尚未招募不适用

Comparison of Supra Inguinal Fascia Iliaca Block versus Femoral Nerve Block under Ultrasound guidance as analgesia before Central neuraxial block in the sitting position for Fracture Neck of Femur Surgery –A Prospective Randomized Clinical Trial in Tertiary Care Centre.

Dr Nisheed Joseph1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年10月20日最近更新:

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
To observe the effectiveness of Supra Inguinal Fascia Iliaca Block and Femoral Nerve Block under Ultrasound guidance as analgesia before Central neuraxial block in the sitting position for Fracture Neck of Femur Surgery. The following objectives are set.

研究概览

简要总结

A Prospective Randomized Clinical trial, double blinded, to observe the effectiveness of Supra Inguinal Fascia Block and Femoral Nerve Block under Ultrasound guidance as analgesia before Central Neuraxial block in the sitting position for 60 patients for Fracture Neck of Femur Surgery in a tertiary centre for a duration of 1 year.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Investigator Blinded

入排标准

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

入选标准

  • 1.Age 18 and above 2.Patients with a fracture neck femur, undergoing surgery under the subarachnoid block, 3.ASA physical status I and II.

排除标准

  • 1.Patient refusal 2.Known hypersensitivity to local anesthetic agents of the amide type 3.Anticoagulant therapy (warfarin/heparin infusion).
  • 4.Clotting disorders [international normalized ratio (INR) or activated partial thromboplastin time ratio (APTR)] more than 1.5, Platelets less than 80,000/microL 5.Previous femoral vascular surgery 6.Hepatic Impairment 7.Debilitated or acutely ill patients 8.Glasgow Coma Scale (GCS) less than 12/15.

结局指标

主要结局

To observe the effectiveness of Supra Inguinal Fascia Iliaca Block and Femoral Nerve Block under Ultrasound guidance as analgesia before Central neuraxial block in the sitting position for Fracture Neck of Femur Surgery. The following objectives are set.

时间窗: The patient will be assessed for pain with Visual Analogue Scale at 0, 2, 5, 10, 15, 20min, and after giving a sitting position and the time will be noted with Zero being the time of giving block.

To compare the time required for the onset of sensory block after both techniques.

时间窗: The patient will be assessed for pain with Visual Analogue Scale at 0, 2, 5, 10, 15, 20min, and after giving a sitting position and the time will be noted with Zero being the time of giving block.

次要结局

  • 1.To identify the dermatomal coverage of the block (femoral, obturator, and lateral femoral cutaneous nerve) after both techniques(2.To assess the adequacy of patient positioning for administering central neuraxial block after both techniques.)

研究者

发起方
Dr Nisheed Joseph
申办方类型
Other [self]

研究点 (1)

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