Skip to main content
Clinical Trials/CTRI/2019/01/017060
CTRI/2019/01/017060
Completed
未知

The effect of preoperative dexmedetomidine nebulization on hemodynamic response to laryngoscopy and intubation:placebo controlled randomized trial

Dr Satyajeet Misra0 sites120 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Dr Satyajeet Misra
Enrollment
120
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
January 9, 2020
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Dr Satyajeet Misra

Eligibility Criteria

Inclusion Criteria

  • Adult patients posted for elective surgery will be recruited into the trial after obtaining their written informed consent. The dexmedetomidine group will receive nebulization with 1 microgram/kg dexmedetomidine diluted in 3\-4 ml normal saline 30 minutes before induction of anaesthesia. Heart rate and blood pressure responses to laryngoscopy and intubation will be recorded for 10 minutes after laryngoscopy. The normal saline group (control) will receive nebulization with normal saline (3\-4 ml) 30 minutes before induction of anaesthesia and heart rate and blood pressure responses to laryngoscopy and intubation will be recorded for 10 minutes after laryngoscopy.

Exclusion Criteria

  • Patients who undergo emergency surgeries, have known or unanticipated difficult airway and those who are on anti\-hypertensive medications will be excluded from the trial.

Outcomes

Primary Outcomes

Not specified

Similar Trials