A Cross Sectional Study Comparing the Effects of Sevoflurane and Desflurane in adults patients undergoing General Anesthesia with Laryngeal Mask Airway
Overview
- Phase
- Post Marketing Surveillance
- Status
- Completed
- Sponsor
- Department of Anesthesiology
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- To observe and compare group A and B regarding the total volume of the inhalational agent, namely Sevoflurane or Desflurane used, total dose of the analgesic drug requirement, intraoperative hemodynamic stability, oxygen saturation, postoperative recovery score, and postoperative side effects, if any, will be assessed and documented for comparison
Overview
Brief Summary
This research aims to evaluate and compare the clinical performance of two inhalational anaesthetic agents—sevoflurane and desflurane, in adult patients scheduled for elective surgical procedures under general anaesthesia (GA) using a laryngeal mask airway (LMA). The study will assess key perioperative parameters, including the duration of surgery, intraoperative Oxygen saturation, Haemodynamic stability based on heart rate, blood pressure, mean arterial pressure and postoperative recovery characteristics based on recovery score and side effects such as nausea, vomiting and delirium.
The goal is to determine which agent offers superior outcomes in terms of anaesthetic efficiency, patient safety, and recovery quality.
Study Design
- Study Type
- Pms
- Allocation
- Na
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •ASA physical status I and II Patients scheduled for elective surgery under GA with LMA Patient is willing to participate in the research.
Exclusion Criteria
- •ASA physical status III and above Pregnant patients, paediatric patients Patient scheduled for emergency surgeries Patient with a history of smoking, chronic alcoholism, drug abuse, and psychiatric disorder Patient refusal.
Outcomes
Primary Outcomes
To observe and compare group A and B regarding the total volume of the inhalational agent, namely Sevoflurane or Desflurane used, total dose of the analgesic drug requirement, intraoperative hemodynamic stability, oxygen saturation, postoperative recovery score, and postoperative side effects, if any, will be assessed and documented for comparison
Time Frame: Before starting the procedure, the baseline parameters of vital signs, SpO2, Heart rate, blood pressure, ECG, and temperature will be assessed. After every 10 minutes till the end of the surgery duration of surgery post post-operative recovery score, and once the patient recovers from General anaesthesia, all these parameters will be assessed and compared between the two groups
Secondary Outcomes
- Nausea, Vomiting, Sore throat(Hourly for 4hrs then after 24hrs)
Investigators
Ms A Jayaprabha
BIHER university