跳至主要内容
临床试验/CTRI/2025/07/091612
CTRI/2025/07/091612尚未招募不适用

A Randomized control study to evaluate the efficacy of Dual Sub-sartorial Block in managing post operative pain in patients undergoing unilateral Total Knee Replacement.

Manipal hospitals1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2025年8月21日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
44
试验地点
1
主要终点
To understand the analgesic efficacy of dual sub sartorial block by evaluating the post operative pain score (NRS) and Patient controlled analgesia demands in 2 groups of patients (Adductor canal block and dual sub sartorial block) in patients undergoing total knee replacement surgery under sub arachnoid block

研究概览

简要总结

A Randomized control study to evaluate the efficacy of dual sub sartorial block in managing post operative pain in patients undergoing unilateral total knee replacement.

Hypothesis

Dual sub sartorial block facilitates adequate post operative pain management and reduction of opioid consumption in asa II and ASA III patients undergoing unilateral TKR under sub arachnoid block

Aim

To understand the analgesic efficacy of dual sub sartorial block by evaluating post operative pain scores and opioid consumption in 2 groups of patients. dual sub sartorial block vs adductor canal block.

To assess consumption of rescue analgesia

To assess sensory deficit in both groups of patients

Study duration

July 2025 to Dec 2025

single center prospective open label, randomized 2 groups post assessment clinical study

inclusion criteria

ASA II III

Age 30y  75y

patients undergoing unilateral TKR under SAB

Exclusion criteria

patient refusal to participate in the study

Allergic to local anasthetic

asa IV

Bilateral tkr

surgery under general anasthesia

sample size- 44

Group A

22 patients receiving dual sub sartorial block

Group B

22 patients receiving adductor canal block

statistical method

Chi square fisher exact test student t test or any other suitable method at the time of data analysis

software SPSS22  R Environment MS Excel and Word

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
30.00 Year(s) 至 75.00 Year(s)(—)
性别
All

入选标准

  • ASA II/III
  • Patients undergoing unilateral total knee replacement
  • Anesthetic management plan of sub arachnoid block.

排除标准

  • Patient refusal to participate in the study
  • Patient allergic to the Local anesthetic used in the study
  • ASA IV patients
  • Patients undergoing bilateral TKR
  • Anesthetic management plan of General anesthesia.

结局指标

主要结局

To understand the analgesic efficacy of dual sub sartorial block by evaluating the post operative pain score (NRS) and Patient controlled analgesia demands in 2 groups of patients (Adductor canal block and dual sub sartorial block) in patients undergoing total knee replacement surgery under sub arachnoid block

时间窗: NRS and PCA demands will be compared at 0 hours, 6 hours, 12 hours and 24 hours

次要结局

  • 1. To assess consumption of rescue analgesia in the 2 aforementioned groups of patients.(2. To assess sensory deficit in the 2 aforementioned groups of patients.)

研究者

申办方类型
Private hospital/clinic
责任方
Principal Investigator
主要研究者

Tejaswini

MANIPAL HOSPITAL OLD AIRPORT ROAD

研究点 (1)

Loading locations...

相似试验