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Clinical Trials/IRCT201306181951N3
IRCT201306181951N3Completed未知

The effect of preoperative intravenous tranexamic acid adminstration on the amount of blood loss in women underwent hysterectomy

Tehran University of Medical Sciences , Deputy of Research0 sites106 target enrollmentStarted: TBDLast updated:
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Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
106
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
no limit to no limit (—)
Sex
Female

Inclusion Criteria

  • •Uterine size <14 cm, hysterectomy for benign pathology, uterine prolapsed and abnormal uterine blooding. Exclusion criteria: History of previous myomectomy, coagulation disorder , history of abnormal coagulation test, thrombophilie, coagulopathy, cardiovascular, tromboemboli and ceasar, renal and liver dysfunction and patients with an allergy to tranexamic acid and BMI>30.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Tehran University of Medical Sciences , Deputy of Research

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