A CLINICAL TRIAL TO COMPARE THE EFFECT OF ADDITION OF LOW DOSE OF SUCCINYLCHOLINE TO PROPOFOL OR ETOMIDATE ON THE EASE OF I-GEL INSERTION IN PATIENTS UNDER GENERAL ANESTHESIA.
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/07/055017
- Lead Sponsor
- DR NAVEEN SANTHOSH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients weighing between 40kg to 80kg.
ASA grades 1, 2 and 3 patients of either sex, scheduled for electives surgeries under GA lasting for not more than 2 hours.
The patient should be willing to provide consent.
Exclusion Criteria
Pharyngeal pathology.
Any anatomical abnormality of mouth, pharynx and larynx.
Risk of aspiration (History of gastroesophageal reflux or upper gastrointestinal surgery).
Full stomach (pregnancy, hiatal hernia),
high airway resistance difficult airway, low pulmonary compliance (severe obesity).
previous history of hypersensitivity to any of study drugs previous history of malignant hyperthermia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method