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Clinical Trials/TCTR20191125001
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.

Phramongkutklao Hospital0 sites120 target enrollmentNovember 25, 2019

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.

Registry
who.int
Start Date
November 25, 2019
End Date
November 1, 2019
Last Updated
last year
Study Type
Interventional
Sex
All

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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