A comparative study on the effect of pre incisional versus postoperative peritonsillar infiltration of 0 point 75 percentage ropivacaine among paediatric patients undergoing coblation tonsillectomy.
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- 1 The outcomes to be measured Pain scoring will be done using the FACES pain scale scale at 4 coma 6 coma 24 hours post operative and day 7 of post operative day
研究概览
简要总结
This study aims to compare the effect of pre incisional verses post operative peritonsillar infiltration of 0 point 7 percent ropivacaine on post tonsillectomy pain in pediatric patients undergoing coblation tonsillectomy full stop post operative pain is a major cause of morbidity following tonsillectomy in children and may delay oral intake and recovery full stop Although local infiltration analgesia has been used to reduce pain limited evidence exists regarding the optimal timing of ropivacaine infiltration especially in coblation tonsillectomy full stop
This prospective study will include children aged 3 to 17 years diagnosed with chronic tonsillitis and planned for coblation tonsillectomy full stop Participants will be randomized into two groups full stop Group A will receive preincisonal peritonsillar infiltration of 0 point 75 percent ropivacaine at a dose of 0 point 2 milgram per kilogram full stop Group B will receive post operative infiltration of the same dose full stop Post operative pain will be assessed using Wong Baker FACES pain scale at 4 hours coma 6 hours coma 24 hours and on the seventh post operative day full stop Time to initiation of oral intake and parental satisfaction will also be recorded full stop
The study aims to determine whether the timing of ropivacaine infiltration provides better postoperative pain relief and facilitates early recovery in children undergoing coblation tonsillectomy full stop
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- None
入排标准
- 年龄范围
- 3.00 Year(s) 至 17.00 Year(s)(—)
- 性别
- All
入选标准
- •Patients with a diagnosis of Chronic tonsilitis fulfilling the Paradise guideline.
排除标准
- •Procedure other than Tonsillectomy Peritonsillar abscess Bleeding disorders Allergy to Ropivacaine.
结局指标
主要结局
1 The outcomes to be measured Pain scoring will be done using the FACES pain scale scale at 4 coma 6 coma 24 hours post operative and day 7 of post operative day
时间窗: 4 coma 6 coma 24 hours post operative and day 7 of post operative day
2 The time at which patients could tolerate
时间窗: 4 coma 6 coma 24 hours post operative and day 7 of post operative day
oral feeds will also be documented
时间窗: 4 coma 6 coma 24 hours post operative and day 7 of post operative day
3 Parental satisfaction regarding the pain outcomes will also be noted
时间窗: 4 coma 6 coma 24 hours post operative and day 7 of post operative day
次要结局
未报告次要终点
研究者
Bhagyashree Padickal
Al Azhar Medical Collage and Super Speciality Hospital
