Comparison of parasternal block given before and after surgery for postoperative pain relief in adult cardiac surgical patients
Not Applicable
Completed
- Registration Number
- CTRI/2018/06/014574
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Elective cardiac surgeries through median sternotomy
Exclusion Criteria
1.history of previous cardiac surgery
2.chronic kidney disease
3.chronic liver disease
4.left ventricular ejection fraction lessthan 35%
5.patients on mechanical ventilator support or inotropes or intra aortic balloon pump preoperatively
6.pregnant and lactating mothers
7,patients who are allergic to study drugs and addicted to narcotis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess and compare the efficacy of preincisional and postincisional parasternal intercostal block on postoperative analgesic requirement in patients undergoing cardiac surgeryTimepoint: 24 hours after shifting to IC
- Secondary Outcome Measures
Name Time Method 1.To assess and compare intraoperative and postoperative hemodynamic stability after preincisional and postincisional parasternal block <br/ ><br>2.To compare duration of postoperative mechanical ventilation after preincisional and postincisional parasternal block <br/ ><br>3.To compare postoperative Visual Analogue Scale(VAS) pain scores after preincisional and postincisional parasternal block <br/ ><br>Timepoint: 1.Heart rate and mean arterial blood pressure will be recorded intraoperatively at baseline, skin incision, sternotomy and sterna retractor placement and post operatively at 0,2,4,6,8,12,24 hours after shifting to ICU <br/ ><br>2.Immediately after extubation in ICU <br/ ><br>3.VAS score will be noted at the time of first spontaneous eye opening and 12,16,20 and 24 hours after shifting to IC