A study to compare between two medical devices for ease of securing airway in small children who are being operated using general anaesthesia.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/03/032076
- Lead Sponsor
- All India Institute Of Medical Sciences Patna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA physical status I and II
ages 6 months to 10 years
weighing 5 to 30 kg
patients undergoing elective surgeries under general anesthesia
Exclusion Criteria
Refusal by the guardian
Anticipated difficult airway
Children who had previously failed conventional direct laryngoscopy.
History of cardiopulmonary disease
Weight-for-height greater than >3 standard deviations above WHO Child Growth Standards median( in age < 5 years) or BMI >30 (in age > 5 years)
Presence of mass/lesion in the airway
Patient posted for emergency procedures
Head and Neck surgery
Any surgical procedure with expected postoperative ICU admission
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method percentage of successful blind endotracheal intubation in a single attempt.Timepoint: after placing lma followed by successful attempt of intubation will be recorded in the intraoperative period.
- Secondary Outcome Measures
Name Time Method peak pressure, the number of attempts required for successful placement of SAD,the glottic view through fiberoptic bronchoscope, the time required to successfully intubate the patient.Timepoint: To be assessed after securing supraglottic device and endotracheal intubation.The post anesthesia related problems are to be assessed after surgery in the post anaesthesia care unit and after 24 hours after.