Study comparing the difference between Propofol & Etomidate in causing changes to vital parameters of trauma patients while facilitating tracheal intubation for artificial breathing
Phase 4
- Conditions
- Health Condition 1: T149- Unspecified injury
- Registration Number
- CTRI/2020/09/027812
- Lead Sponsor
- Dr Sampurnand Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Inclusion criteria for patients :
Patients of either sex with age between 20 to 60 years and body weight 30 to 80 kg belonging to ASA grade 1 and 2, admitted in trauma center receiving no narcotics or sedative drug and who are hemodynamically stable before induction will be included in the study
Exclusion Criteria
Exclusion criteria :
Patient who refuse to participate, patients in shock or if they have any H/o convulsion, allergy to the drug used, respiratory, cardiac, hepatic, or renal dysfunction or if they belong to ASA Grade 3 or 4 will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine any difference in objective hemodynamic response (HR, SBP, DBP, MAP) due to IV Propofol and IV Etomidate used during laryngoscopy and intubation in trauma patients.Timepoint: Baseline values of bp ,pulse and MAP ,then one minute after laryngoscopy,then after 5 minutes.
- Secondary Outcome Measures
Name Time Method To determine any difference in objective hemodynamic response (HR, SBP, DBP, MAP) due to IV Propofol and IV Etomidate used during laryngoscopy and intubation in trauma patients.Timepoint: Baseline values of bp ,pulse and MAP ,then one minute after laryngoscopy,then after 5 minutes.