The Efficacy of Ultrasound-guided Bilateral Superficial Cervical Plexus Block on Postoperative Pain Relief in Patients Undergoing Neck Surgeries, Prospective Randomized Controlled Study.
试验速览
- 阶段
- 4 期
- 状态
- 进行中（未招募）
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- analgesic effect of SCPB postoperative in neck surgeries
研究概览
简要总结
analgesic effect of superficial cervical plexus block by using ultrasound in patients undergoing neck surgeries
详细描述
The efficacy of ultrasound-guided bilateral superficial cervical plexus block on postoperative pain relief in patients undergoing neck surgeries, prospective randomized controlled study,To assess the analgesic efficacy of bilateral superficial cervical plexus block in reducing post-operative pain following neck surgery, decrease total opoid consumption during first 24h post operative.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •The study include all patients between 18 and 60 years of age who underwent elective neck surgery under general anesthesia
排除标准
- •1. Patient refusal .
- •Patient with significant neurological , psychological disease .
- •patient known allergy to local anesthesia .
- •Patient uncorrected coagulapathy or anticoagulant therapy .
- •Patient with sever neck deformity .
- •Patient with infection at site of injection .
- •Patient with sever respiratory disease .
- •patients with regular use of analgesic medications
研究组 & 干预措施
Group will take the block
干预措施: superficial cervical plexus block guided by ultrasound with bupivacaine (Procedure)
Controlled group
干预措施: Paracetamol (500 mg) tablets (Drug)
结局指标
主要结局
analgesic effect of SCPB postoperative in neck surgeries
时间窗: in the 24h postoperative
To assess the analgesic efficacy of bilateral superficial cervical plexus block in postoperative pain following neck surgery assed by Visual Analog Scale
Analgesic effect of bilateral superficial cervical plexus block in postoperative neck surgeries
时间窗: within the first 24 hours postoperatively
To assess the analgesic efficacy of bilateral superficial cervical plexus block on postoperative pain following neck surgery, as measured by the Visual Analog Scale Pain was assessed using the Visual Analog Scale (VAS; 0 = no pain, 10 = worst imaginable pain) at 1, 4, 8, 12, and 24 hours postoperatively.
次要结局
- Total opioid consumption(in the 24 h postoperative)
- Total opioid consumption(within the first 24 hours postoperatively)
研究者
Mohamed Sabry Mahmoud
Resident of Anesthesia, Intensive Care and Pain management Sohag university hospital.
Sohag University