Comparison between thiopentone and propofol regarding hemodynamics during induction of GA
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/01/048906
- Lead Sponsor
- Health and family welfare department
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade I, II, III undergoing elective surgery under general
anaesthesia
Giving positive consent
Undergoing surgical procedures - general surgery urosurgery orthopaedic surgery neurosurgery ENT surgery under general anaesthesia
Exclusion Criteria
Patients giving negative consent
Age <18 years and > 60 years
Patient having recent URTI, any drug allergy
Anticipated difficult airway, restricted mouth opening, h/o regurgitation
Patients having neuromuscular disorder and neurological symptoms, pathology of oropharynx, neck and upper GIT
Patients having hypertension
Pregnancy
Patients on medication affecting heart rate and blood pressure
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To analyse how effective Propofol and Thiopental sodium are to maintain Hemodynamic stability during induction and to compare changes in pulse rate, diastolic blood pressure, systolic blood pressure, mean arterial pressure of the two groupsTimepoint: All parameters mentioned above are monitored at 0, 1,3,5,10,15 minutes after induction
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI