A comparison of analgesic efficacy of ultrasound guided External Oblique Intercostal Plane Block with IV opioids vs only IV opioids in pediatric patients undergoing upper abdominal surgeries: A Randomized Clinical Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Total Intraoperative fentanyl consumption
研究概览
简要总结
This is a randomized clinical trial to study the analgesic efficacy of ultrasound guided External Oblique Intercostal Plane Block in pediatric patients undergoing upper abdominal surgeries.Ultrasound guided external oblique intercostal plane block will be given in supine position to all the patients belonging to group I alongwith intravenous opioids and group II will recieve only intravenous opioids. Intraoperative any increase in HR/MAP more than 20% intraoperatively will be treated with additional fentanyl doses of 1 mcg/kg and total intraoperative fentanyl consumption will be noted and compared in the two groups. Both groups will be compared with respect to Postoperative pain score using FLACC score at 1, 4, 8, 16, 24 hours at rest, time to first rescue analgesic administration , total Tramadol consumption 24 hours postoperatively, side effect likes nausea, vomiting and sedation and local anaesthetic toxicity
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant, Investigator and Outcome Assessor Blinded
入排标准
- 年龄范围
- 2.00 Month(s) 至 7.00 Year(s)（—）
- 性别
- All
入选标准
- •ASA I and II patients scheduled for upper abdominal surgeries with unilateral incisions.
排除标准
- •Parent refusal to participate in the study Patients hypersensitive to study medications Patients with developmental or mental delay Skin lesions or infection at the planned site of needle insertion.
结局指标
主要结局
Total Intraoperative fentanyl consumption
时间窗: 5, 30, 60, and 90 minutes after skin incision and at the end of surgery
次要结局
- Postoperative pain score using FLACC score at 1, 4, 8, 16, 24 hours at rest.(To determine time to first rescue analgesic administration)