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Clinical Trials/IRCT20200526047573N1
IRCT20200526047573N1
Completed
Phase 3

Comparison of the sedation effect of propofol with lidocaine spray versus isolated propofol admission during upper GI endoscopy in elective and outpatient patients

Babol University of Medical Sciences0 sites160 target enrollmentTBD
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ConditionsDiseases of upper digestive system which need endoscopy.Gastric ulcer

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Diseases of upper digestive system which need endoscopy.
Sponsor
Babol University of Medical Sciences
Enrollment
160
Status
Completed
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Patient age between 20 to 65 years old
  • •Patients requiring upper gastrointestinal endoscopy

Exclusion Criteria

  • •Psychological disease
  • •Swallowing Disorders (Myasthenia gravis and Alzheimer's)
  • •Cardiac Disease
  • •Low blood pressure
  • •Bradycardia
  • •Hepatic Failure
  • •Kidney Disease

Outcomes

Primary Outcomes

Not specified

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