Impact on intraoperative blood pressure and heart rate during surgery with propofol versus sevoflurane anesthesia.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/08/072486
- Lead Sponsor
- Sir Ganga Ram Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with laryngeal pathology undergoing microlaryngeal surgery (MLS)
ASA physical status I and II
Exclusion Criteria
1.ASA GR III AND IV (uncompensated cardiovascular, hepatic, or renal disease)
2.Psychiatric or neurological disorder
3.Uncontrolled endocrine disease (diabetes mellitus, hypothyroidism)
4.Known allergy or hypersensitivity to the study drug.
5.Drug dependence or substance abuse
6.Refusal to informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Haemodynamic changes during suspension laryngoscopy (heart rate, Systolic blood pressure)Timepoint: At pre-induction, post-induction, post endotracheal intubation, every 3 minutes post insertion of rigid laryngoscope till its removal and every 30 minutes (for first 2 hours)
- Secondary Outcome Measures
Name Time Method Frequency of adverse haemodynamic effects <br/ ><br>Use of rescue drugs for maintaining haemodynamicsTimepoint: pre induction, post-induction, post endotracheal intubation, every 3 minutes post insertion of rigid laryngoscope till its removal & every 30 minutes (for first 2 hours)