SPACING TIME INTERVALS OF FENTANYL, TO DECREASE REQUIREMENT OF PROPOFOL IN GENERAL ANAESTHESIA
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2023/01/049283
- Lead Sponsor
- SDM Medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients willing to participate in the study
2.Patients undergoing elective surgery under general anaesthesia with endotracheal intubation
3.ASA physical status 1 and 2
4.Patients aged 18-60 years of either sex
1.patient refusal
2.BMI more than or equal 30kg/m2
3.anticipated difficult airway
4.history of allergy to drugs like propofol
5.history of alcohol/drug use
6.Respiratory,cerebrovascular, renal and cardiovascular diseases including uncontrolled hypertension
7.Receiving any drugs likely to affect requirement of propofol /hemodynamic changes
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.