ovel use of Erector spinae block during laparoscopic surgeries
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/09/036754
- Lead Sponsor
- DrDYpatil medical collegehospital and research centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
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
Exclusion Criteria
Asa 3 or more
Patients posted for emergency procedure
Major neurological,cardiac,respiratory,metabolic,renal,hepatic diseases with coagulation abnormalities
Cardiac comorbidities
Patients refusal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the effectiveness of erector spinae block for haemodynamic stability during laparoscopic surgeriesTimepoint: 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
- Secondary Outcome Measures
Name Time Method The amount of Fentanyl required intraoperatively and the amount of inhalational agent required intraoperatively will be measured.Timepoint: 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.