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Clinical Trials/CTRI/2018/01/011417
CTRI/2018/01/011417
Completed
未知

A randomized clinical trial to compare the effectiveness of dexmedetomidine versus propofol-fentanyl combination for sedation during awake fiberoptic nasotracheal intubation

Dr Radha M0 sites60 target enrollmentTBD
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ConditionsHealth Condition 1: null- Difficult Airway

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- Difficult Airway
Sponsor
Dr Radha M
Enrollment
60
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
March 5, 2017
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Dr Radha M

Eligibility Criteria

Inclusion Criteria

  • •1\.ASA grade 1 to 3
  • •2\.Patients scheduled for elective awake fiberoptic intubation.

Exclusion Criteria

  • •1\.Baseline heart rate \<60/min,any type of atrioventricular block on the ECG,heart failure
  • •2\.Emergency surgery,Pregnancy
  • •Liver cirrhosis
  • •3\.Thrombocytopenia or coagulopathy contraindicating nasal intubation.
  • •4\.Known alcoholic or drug abusers,allergy to the drugs involved in the study

Outcomes

Primary Outcomes

Not specified

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