COMPARISION OF TWO AIRWAY DEVICES IN PATIENTS RECEIVING GENERAL ANAESTHESIA
Not Applicable
Completed
- Conditions
- Health Condition 1: L99- Other disorders of skin and subcutaneous tissue in diseases classified elsewhere
- Registration Number
- CTRI/2019/08/020691
- Lead Sponsor
- pondicherry institute of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
1.Patients coming under American Society of Anesthesiologists grade I or II
ASA I- Normal healthy individuals
ASA II-Patient with mild systemic disease well compensated which include current smoker, mild lung disease, social drinker, well controlled Diabetes mellitus and hypertension.
2.Age : above 18 yrs. and below 65yrs
3.Mallampati grade I & II.
4.Surgeries lasting for 1 to 3 hours (like short gynaecologic procedures, hernioplasties, incision and drainage and fibroadenoma excision.)
Exclusion Criteria
1.Emergency surgeries
2.Patients with known gastrointestinal reflux, sore throat, upper respiratory airway infections.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate igel and baska maskâ?? oropharyngeal sealing pressure (OSP)Timepoint: 2021 may
- Secondary Outcome Measures
Name Time Method 1.The ease of insertion. <br/ ><br>2.To determine the success rate of insertion based on positioning of the igel and baska mask <br/ ><br>3.To detect the hemodynamic responses induced by airway insertion (blood pressure, heart rate, oxygen saturation and end-tidal carbon dioxide (EtCO2)). <br/ ><br>4.The incidence of postoperative complications such as the presence of laryngospasm on emergence, blood on the mask, sore throat. <br/ ><br>Timepoint: INTRA OP AND POST OP TILL FIRST 24HRS