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Clinical Trials/IRCT20200501047254N3
IRCT20200501047254N3RecruitingPhase 2

Examining the effect of using the drug propofol in anesthesia on the blood fat and bicarbonate ion levels in patients undergoing spinal surgery

Gonabad University of Medical Sciences0 sites58 target enrollmentStarted: TBDLast updated:
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Conditions

Trial Snapshot

Phase
Phase 2
Status
Recruiting
Sponsor
Enrollment
58
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20 years to 70 years (—)
Sex
All

Inclusion Criteria

  • •Informed consent of the patient to participate in the research
  • •Patient age between 20 and 70 years
  • •Patient with ASA class I and II
  • •Duration of surgery at least 4 hours
  • •Blood fat before the operation should be at a normal level (less than 200).
  • •Blood pH should be at a normal level before the operation.
  • •Do not have underlying diseases including liver and blood diseases.
  • •The patient should not be a candidate for surgery due to trauma and in emergency conditions.
  • •The patient does not have a history of drug addiction.
  • •The patient should not be overweight or obese.
  • •The patient does not have a history of taking antipsychotic drugs

Exclusion Criteria

  • •Patient withdrawal from participating in research
  • •Occurrence of heart and respiratory problems before the start of the plan

Investigators

Sponsor
Gonabad University of Medical Sciences

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