COMPARISION OF TWO LARYNGEAL MASK AIRWAY DEVICES IN MANAGEMENT OF PATIENTS UNDERGOING OPERATIVE PROCEDURE
Phase 3
- Conditions
- Health Condition 1: K80- CholelithiasisHealth Condition 2: N97- Female infertilityHealth Condition 3: N84- Polyp of female genital tractHealth Condition 4: H66- Suppurative and unspecified otitismediaHealth Condition 5: N63- Unspecified lump in breast
- Registration Number
- CTRI/2022/02/039934
- Lead Sponsor
- Department of Anaesthesiology and Critical Care Jawaharlal Nehru Medical College AMU Aligarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Written and informed consent from the patient
2.ASA grade 1 and 2 patients
3.All Mallampatti grades
Exclusion Criteria
1.Mouth opening <2.5 cm
2.Patients with known difficult airway
3.Potentially full stomach patients (trauma, morbid obesity, pregnancy, GERD).
4.Cervical spine fracture or instability
5.History of allergy to latex
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Insertion timeTimepoint: Insertion time shall be calculated from the time of introduction of the device into the mouth till confirmation by capnographic tracing.
- Secondary Outcome Measures
Name Time Method 1.To compare the ease of insertion of both the devices. <br/ ><br>2.To compare the hemodynamics response i.e, Heart Rate and Mean Arterial Blood Pressure (MABP) after insertion. <br/ ><br>3.To compare the incidence of complications. <br/ ><br>Timepoint: Grade 1: No resistance to insertion in the pharynx. <br/ ><br>Grade 2: Mild resistance to insertion. <br/ ><br>Grade 3: Moderate to severe resistance to insertion. <br/ ><br>Grade 4: Failed insertion. <br/ ><br>Heart rate and MABP shall be recorded from a standard multichannel monitor.(pre induction, post insertion, and after 3 minutes,5 minutes and 10 minutes). <br/ ><br>Complications shall be assessed by presence or absence of blood on device after removal and post operative sore throat <br/ ><br> <br/ ><br>