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临床试验/CTRI/2021/09/036754
CTRI/2021/09/036754尚未招募3 期

Efficacy of erector spinal block during laparoscopic surgeries

DrDYpatil medical collegehospital and research centre1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2021年9月27日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
To determine the effectiveness of erector spinae block for haemodynamic stability during laparoscopic surgeries

研究概览

简要总结

To determine the effectiveness of erector spinae block for haemodynamic stability during laparoscopic surgeries Performed under general anaesthesia using 20 cc of 0.25 bupivacaine

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Investigator 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

  • •Asa grade 1 and 2 Patients undergoing laparoscopic surgeries under general anaesthesia Haemodynamically stable patients with all routine investigations within normal limits without comorbidities Patients not on any cardiac related drugs.

排除标准

  • •Asa 3 or more Patients posted for emergency procedure Major neurological,cardiac,respiratory,metabolic,renal,hepatic diseases with coagulation abnormalities Cardiac comorbidities Patients refusal.

结局指标

主要结局

To determine the effectiveness of erector spinae block for haemodynamic stability during laparoscopic surgeries

时间窗: Heart rate, systolic and diastolic blood pressure will be monitored at baseline, at induction of pneumoperitoneum, and every 10 mins thereafter untill the completion of surgery

次要结局

  • The amount of Fentanyl required intraoperatively and the amount of inhalational agent required intraoperatively will be measured.(The amount of fentanyl required intraoperatively, given in aliquots whenever heart rate or blood pressure increases 20% above the baseline values will be recorded for the duration of surgery. The amount of inhalational agent (Isoflurane) used intraoperatively during the period of surgery will be measured.)

研究者

发起方
DrDYpatil medical collegehospital and research centre
申办方类型
Research institution and hospital

研究点 (1)

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