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Clinical Trials/IRCT20210415050983N3
IRCT20210415050983N3
Not yet recruiting
Phase 3

Comparison of effectiveness of Different doses of prophylactic intravenous fibrinogen versus normal saline on intraoperative bleeding in posterior spinal fusion surgery

Shahid Beheshti University of Medical Sciences0 sites40 target enrollmentTBD
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Conditionsumbar Discopathy.Intervertebral disc disorders with myelopathy, thoracolumbar regionM51.05

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
umbar Discopathy.
Sponsor
Shahid Beheshti University of Medical Sciences
Enrollment
40
Status
Not yet recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • •No history of drug allergy
  • •No history of thromboembolism and coagulation disorders
  • •No history of liver or kidney failure
  • •No history of heart disease and hypertension
  • •Patient consent to participate in the study

Exclusion Criteria

  • •use of anticoagulants
  • •History of blood disorders and coagulopathy
  • •History of liver disease
  • •History of chronic kidney disease and creatinine greater than 2mg / dl
  • •History of thromboembolic events at any time

Outcomes

Primary Outcomes

Not specified

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