Ultrasound guided llioinguinal/llio-hypogastric nerve block vs transverse abdominis plane block for pain management following inguinal hernia repair surgery:A randomised clinical trial
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- 1) Severity of pain using Visual Analogue Scale (VAS)
研究概览
简要总结
This study is a randomised, parallel group, clinical trial comparing the effectiveness of two blocks
i.e ultrasound guided transversus abdominis plane block versus ilioinguinal/ iliohypogastric block for
postoperative analgesia in patients undergoing inguinal surgeries, as measured by duration of
analgesia and pain score in 24 hours following surgery. The primary outcome of the study is to
record the severity of pain using Numerical rating scale and time to request of first analgesia i.e
the time elapsed between the end of surgery to 1st dose of analgesia. The secondary outcome is
to see the total no. of analgesic doses of opioids and NSAIDs in 24 hours following surgery and to
see any side effects like nausea, vomiting and shivering occurring after the procedure.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •patients between age group of 18 years to 60years who are undergoing inguinal hernia repair in elective OT 2) ASA class 1 & 2 3) patients who are willing to participate and provide a willing written informed consent.
排除标准
- •patients with any chronic medical illness 2) history of any bleeding disorders 3) patients allergic to any of these drugs.
结局指标
主要结局
1) Severity of pain using Visual Analogue Scale (VAS)
时间窗: 1) Severity of pain using Visual Analogue Scale (VAS) at 1,2,6,12 and 24 hrs of surgery. | 2)
2) Time to 1st request of analgesia
时间窗: 1) Severity of pain using Visual Analogue Scale (VAS) at 1,2,6,12 and 24 hrs of surgery. | 2)
次要结局
- 1) Total number of analgesic doses of opioids and NSAIDS in 24 hours following(surgery)
研究者
Dr Neeraj Badyal
Government Medical College Kathua