Comparison of efficacy and outcome of airway device-Proseal Laryngeal mask airway with Endotracheal tube under low flow anesthesia.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Adult ASAPS-I and II patients
- Registration Number
- CTRI/2018/05/014325
- Lead Sponsor
- Medical college and SSGHospital Baroda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1. Weight- 40 to 70 kg
2. ASA PS- I and II
3. Patients Undergoing planned surgeries under GA of Duration of 45-120 minutes.
Exclusion Criteria
1.Patients with likely difficult airway
2.Patients with Gastro esophageal reflux disease
3.Patients with full stomach
4.Patients with known allergy to latex
5.Recent history of sore throat or common cold with in last 10 days
6.Patients with acute or chronic cardiovascular diseases, respiratory diseases, renal or liver insufficiency.
7.Patients who consume alcohol and who smoke
8.Patient not willing to participate in the study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method