CTRI/2024/08/071765尚未招募2/3 期
Comparison of Analgesic Efficacy of Dual Subsartorial Block and Adductor Canal Block with Local Infiltration Analgesia in Patients Undergoing Total Knee Arthroplasty
Vardhman Mahavir Medical College and Safdarjung Hospital1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年8月11日最近更新:
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- To compare the analgesic efficacy of dual subsartorial block and adductor canal block with local infiltration analgesia for complete pain relief using the postoperative visual analog scale in patients undergoing total knee arthroplasty.
研究概览
简要总结
COMPARISON OF ANALGESIC EFFICACY OF DUAL SUBSARTORIAL BLOCK 30 ml Ropivacaine 0.2% with 8 mg dexamethasone (10 ml in the distal femoral triangle and 20 ml in the adductor canal)
AND ADDUCTOR CANAL BLOCK WITH LOCAL INFILTRATION ANALGESIA 60 ml Ropivacaine 0.2% with 8 mg dexamethasone (10ml in the adductor canal and 50 ml local infiltration analgesia)
IN PATIENTS UNDERGOING TOTAL KNEE ARTHROPLASTY
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded
入排标准
- 年龄范围
- 25.00 Year(s) 至 80.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients aged 25-80 years
- •American society of anaesthesiologists (ASA) Grade I – III
- •Elective unilateral TKA with varus knee or mild valgus deformity via medial approach.
排除标准
- •Neurological deficit, cognitive dysfunction, operated limb neuropathy
- •Previously operated patients posted for redo total knee arthroplasty
- •Hypersensitivity to local anaesthetic agent or any of the study medications
- •Inability to understand visual analogue scale (VAS) for pain.
结局指标
主要结局
To compare the analgesic efficacy of dual subsartorial block and adductor canal block with local infiltration analgesia for complete pain relief using the postoperative visual analog scale in patients undergoing total knee arthroplasty.
时间窗: 6 hrly for first 24 hours and 12 hourly till 72 hours postoperatively)
次要结局
- 1. To measure the operated limb strength between groups using Medical Research Council scale every six hourly(6 hrly for first 24 hours and 12 hourly till 72 hours postoperatively))
- 2. To find the timing of first rescue analgesic and calculate total postoperative tramadol consumption between groups(Till 72hrs)
- 3. To determine the sensory duration of the block.(Till discharge)
- 4. To map the site of postoperative knee pain and character of pain .(Till discharge)
- 6. Time to ambulation in the postoperative period.(Till discharge)
- o determine the total postoperative length of hospitalization.(Till discharge)
- To determine patient’s overall satisfaction score at discharge using 0-5 score(At discharge)
研究者
Dr Supreeth L
Vardhman Mahavir Medical College and Safdarjung Hospital
研究点 (1)
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