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临床试验/CTRI/2025/09/094504
CTRI/2025/09/094504尚未招募3 期

Comparison of ultrasound guided dual subsartorial block and local infiltration analgesia for postoperative analgesia after total knee arthroplasty - A randomized comparative study

PONDICHERRY INSTITUTE OF MEDICAL SCIENCES1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2025年9月30日最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
44
试验地点
1
主要终点
To measure the effect of ultrasound guided dual subsartorial block on postoperative analgesia during the first 24hrs in comparison to periarticular infiltration among patients undergoing total knee arthroplasty under spinal anesthesia

研究概览

简要总结

our study if focused on comparing the efficacy of dual subsartorial block as a targeted regional anesthesia technique for total knee replacement arthrioplasty .A direct comparison of the modality with periarticular infiltration remains unexplored in the current literature. therefore our study findlings will have significant implications for orthopaedic surgeons and anaesthesiologist enabling them to choose the most effective analgesic regimen for optimal perioperative pain management

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
30.00 Year(s) 至 85.00 Year(s)(—)
性别
All

入选标准

  • 1.)Patients belonging American Society of Anesthesiologists (ASA) physical status of I-III.
  • 2.)Patients aged 30–85 of either sex.

排除标准

  • 1.)Body mass index (BMI) greater than 35 kg/m2 2.)Severe valgus deformity 3.)Acute/chronic kidney disease 4.)Operative limb neuropathy 5.)Known allergies to local anesthetic agent.

结局指标

主要结局

To measure the effect of ultrasound guided dual subsartorial block on postoperative analgesia during the first 24hrs in comparison to periarticular infiltration among patients undergoing total knee arthroplasty under spinal anesthesia

时间窗: VAS, to measure pain intensity in both the groups in first 24 hrs. | Time for first rescue analgesia and total dose of rescue analgesia | Quadriceps strength | Quality of recovery using QOR – 15 scale | Adverse effects

次要结局

  • To compare the time duration for requirement of first rescue analgesia.

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr SHYAM SUNDER

Pondicherry institute of medical sciences

研究点 (1)

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