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Clinical Trials/IRCT20160307026950N57
IRCT20160307026950N57
Recruiting
Phase 3

Comparison of propofol sedation and lidocaine-propofol combination in patients undergoing bronchoscopy

Esfahan University of Medical Sciences0 sites60 target enrollmentTBD
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ConditionsAnaesthesia.Anaesthetic, unspecifiedY48.4

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Anaesthesia.
Sponsor
Esfahan University of Medical Sciences
Enrollment
60
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Minimum 18 years of age and maximum 60
  • •ASA I or ASA II group of patients
  • •Bronchoscopy candidate either male or female

Exclusion Criteria

  • •Analgesics or Opioid use 24 hours before procedure
  • •Previous use of Beta blockers
  • •Any known allergy to drugs used in this trial
  • •Patients with a past medical history of severe cardiovascular diseases, Asthma, Renal disease, Hepatic disease, chronic respiratory disease
  • •Past history of Drug Allergy
  • •Immunodeficiency
  • •Alcohol consumption 24 hours before procedure
  • •Muscular weakness

Outcomes

Primary Outcomes

Not specified

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