Portal blocks for postoperative pain relief in patients undergoing breast surgery-A Case Control Study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 56
- 试验地点
- 1
- 主要终点
- To evaluate efficacy of portal blocks for post-operative pain management in woman undergoing Breast surgery
研究概览
简要总结
After obtaining institutional ethical committee clearance, this case control study is carried out in 60 female patients (American Society of Anesthesiology [ASA] physical status 1,2) undergoing breast surgery during the period of January 2024 to June 2024.
Patients are allocated into two groups as Group A and Group P using computer generated software.
a)
Group P-Subcutaneous infiltration of mixture of 8ml Injection 0.25% Bupivacaine + 1ml Triamcinolone 40mg + 1ml Injection Clonidine 30mcg.3ml of this mixture is administered in mid-sternal area at the level 4th rib and 3ml in the mid- axillary line of the operated side at the level of 7th rib once the NRS Score is more than or equal to 7.
b) Group A-Paracetamol 1g I.V infusion every 8th hourly and Injection Tramadol 50mg 12th hourly
An independent observer collects the data. NRS score will be documented postoperatively every hourly for first six hours then every 4th hourly till 48 hrs. All patients will be monitored for pain using NRS score and hemodynamics with pulse rate and blood pressure.
If NRS Score >= 7 despite portal block, rescue analgesia is provided with Injection Paracetamol 1g I.V Infusion and Injection Tramadol 50mg I.V
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Double
入排标准
- 年龄范围
- 30.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- Female
入选标准
- •ASA Grade 1,2 2)Age between 30-70 years 3)Female patients undergoing breast surgery.
排除标准
- •Patient Refusal 2) ASA III and above 3) Patient with Coagulation disorders or on anticoagulant and antiplatelet drugs 4) Infection at the site of injection 5) Known allergy to the any of study drugs.
结局指标
主要结局
To evaluate efficacy of portal blocks for post-operative pain management in woman undergoing Breast surgery
时间窗: 20minutes after block, followed by every 2 hourly upto 48 hours
次要结局
- To Evaluate patient satisfaction & effects on hemodynamic parameters(starting from 20 minutes after the block, followed by every 2 hours for 48hours post surgery)
研究者
NamrathaM
Jawaharlal Nehru Medical College