Comparison of success rate of topical versus intravenous lignocaine for insertion of Laryngeal mask airway with propofol
Not Applicable
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2022/11/047181
- Lead Sponsor
- Sawai Mansingh Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients willing to give written informed
consent.
2.Age 18 to 45 years.
3.Patients with ASA grade I and II.
Exclusion Criteria
? patients refusing consent to participate in the study
? patients allergic to propofol and/or lignocaine
? obesity(bmi >30)
? anticipated difficult airway
? Respiratory/cerebriovascular/cardiovascular and renal diseases including hypertension
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Objective of present study is to determine the conditions for LMA insertion.Timepoint: 30 secs after giving Propofol in both the groups respective.
- Secondary Outcome Measures
Name Time Method Mean systolic blood pressure <br/ ><br>Mean diastolic blood pressure <br/ ><br>Mean arterial pressure <br/ ><br>Mean heart rate <br/ ><br>Mean of proportion of cases experiencing coughing, laryngospasm, gagging. <br/ ><br>Timepoint: These parameters were recorded according to scheduled times: <br/ ><br> T0 Base line reading <br/ ><br> T1 Thirty seconds after <br/ ><br> induction with propofol <br/ ><br> T2 one minute <br/ ><br> T3 Two minutes <br/ ><br> T4 Three minutes <br/ ><br> <br/ ><br>