CTRI/2024/04/065794
Not Yet Recruiting
Phase 2
To study and compare the efficacy of preoperative Magnesium Sulphate nebulization with Ketamine nebulization In reducing the incidence and severity of post-operative pharyngolaryngeal complications - A prospective triple blinded randomised controlled Study - NI
dr vaishnav0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
- Sponsor
- dr vaishnav
- Status
- Not Yet Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Males and females between the age group 18\-60 years.
- •2\. ASA class I\-II.
- •3\. Body mass index(BMI) 18\.5\-29\.9\.
- •4\. Undergoing surgeries requiring general anaesthesia with cuffed ETT of duration 60\-120 minutes.
Exclusion Criteria
- •1\. Patient’s refusal participation in study.
- •2\. Haemodynamically unstable patients.
- •3\. History of hypertension, asthma, chronic obstructive pulmonary disease(COPD), cardiovascular disease, renal disease, diabetes mellitus, cerebrovascular disease.
- •4\. Patients having known hypersensitivity to drugs under consideration.
- •5\. Patient with three or more attempts at laryngoscopy or bougie for intubation.
- •6\. Patients who sustained trauma while intubation or nasogastric tube insertion as evidenced by blood on cuff after extubation or blood stained secretions while suctioning before extubation.
- •7\. Patient suffering from active or recent (past 6 weeks) upper airway tract infection (preoperative sore throat, cough) and edema/inflammation noticed during laryngoscopy.
- •8\. Surgery requiring placement of nasogastric tube intraopeartively.
- •9\. Patients already on analgesics or steroids (systemic or inhaled).
Outcomes
Primary Outcomes
Not specified
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