Effects of stellate ganglion block on intraoperative hemodynamic responses to pneumoperitoneum in adult patients undergoing laparoscopic cholecystectomy- Hospital based randomised controlled trail.
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- To assess the effects of the right stellate ganglion block on hemodynamic response to pneumoperitoneum in patients undergoing laparoscopic cholecystectomy
Study Overview
Brief Summary
This is double blinded randomized controlled trial recruiting 60 participants equally divided into two groups of study and control. Study group participants will receive ultrasound guided right sided stellate ganglion block using 10ml of 0.75% Ropivacaine in the preoperatively 15 mins before surgery. Whereas control group participants will receive ultrasound guided right sided stellate ganglion block using 10 ml of normal saline as a placebo. All the participants are induced in under general anesthesia according to standard institutional protocols. Patient baseline vitals will be monitored before the block, during laryngoscopy, intubation, pneumoperitonuem, 5 mins, 10 mins, 15 mins, 20 mins, 30 mins intraoperatively. Heart rate and mean arterial pressure values will be statistically analysed in both the groups to extrapolate the results of the study.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Double
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •ASA physical status 1 and 2 Patients undergoing laparoscopic cholecystectomy Patients belonging to age group of 18 to 60 years.
Exclusion Criteria
- •Patient refusal Patients allergic to ropivacaine Patients with infection at the site of injection.
Outcomes
Primary Outcomes
To assess the effects of the right stellate ganglion block on hemodynamic response to pneumoperitoneum in patients undergoing laparoscopic cholecystectomy
Time Frame: To assess the heart rate, blood pressures at baseline, during laryngoscopy, during pneumoperitoneum, 5 minutes, 10 minutes, 15 minutes, 20 minutes, 30 minutes
Secondary Outcomes
- To assess the stress response to laryngoscopy & endotracheal intubation(Baseline, Laryngoscopy, pneumoperitoneum, 5mins, 10 mins, 15 mins, 20 mins, 30 mins)
Investigators
Rakshitha R
KLE university