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Clinical Trials/IRCT2016122731611N1
IRCT2016122731611N1CompletedPhase 2

Comparison of two ventilation methods volume control & pressure control on blood loss of posterior Spinal fixation surgery

Vice Chancellor for Research and Technology Kashan University of Medical Sciences0 sites78 target enrollmentStarted: TBDLast updated:
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Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
78
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 75 years (—)
Sex
All

Inclusion Criteria

  • •Patients aged 18-75 with physical condition scored 1 or 2 from American Anesthesia Association nominated for elective-fusion posterior spine surgery operation in 3-4 levels, hospitalized for traumatic fracture of the lumbar spine.
  • •Exclusion criteria: Patients with cardiopulmonary disorders; uncontrolled hypertension and diabetes; SCI and coagulopathies patients and patients with BMI more than 35; or treated by aspirin; heparin and warfarin are excluded from the study.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Vice Chancellor for Research and Technology Kashan University of Medical Sciences

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