TCTR20191125001
Completed
Phase 4
Comparison of the effects of intravenous propofol and intravenous propofol with low dose of ketamine on preventing post-extubation cough and laryngospasm in patient awakening from general anesthesia: a prospective randomized clinical trial.
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Prevention of incidence and severity of cough and laryngospasm
- Sponsor
- Phramongkutklao Hospital
- Enrollment
- 120
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •ASA physical status I and II, with airway assessment of Mallampati grade 1 and 2, between the age group of 18\-60 years, scheduled for elective surgeries under general anesthesia.
Exclusion Criteria
- •unwilling patients, history of allergy to any drug, history of bronchial asthma, chronic obstructive pulmonary disease, respiratory tract infection, impaired kidney or liver function, on angiotensin converting enzyme inhibitors, a history of hypersensitivity to local anesthetics, pregnancy and language barrier.
Outcomes
Primary Outcomes
Not specified
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