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The Use of Tranexamic Acid (TXA) Intravenously, to Reduce Blood Loss in Proximal Femur Surgery

H

HaEmek Medical Center, Israel

Status and phase

Withdrawn
Phase 4

Conditions

Femur Surgery

Treatments

Drug: control grup: without Tranexamic Acid (TXA) treatment.
Drug: Tranexamic Acid (TXA) treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT02164565
104-12-EMC

Details and patient eligibility

About

The use of Tranexamic Acid (TXA) intravenously, to Reduce Blood Loss in proximal femur surgery.

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients over 60, who came to the orthopedic department for proximal femur fracture surgery
  • Sound judgment

Exclusion criteria

  • Known hypersensitivity to Tranexamic Acid or component solution provided
  • Subarachnoid hemorrhage
  • Acquired color blindness
  • Myocardial infarction in 12 months before admission
  • Unstable angina
  • Known clotting disorders (Thromboembolic disease in the past, elongated PT and PTT, hypercoagulability),
  • Kidney or liver failure
  • Another situation prostate resection , pathologic fractures according to anamnesis or by imaging
  • Oncology patients
  • Patients on anticoagulation
  • Patients undergoing vascular intervention ( coronary or peripheral ), which was inserted Supporter requires a Dual antiplatelet therapy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Tranexamic Acid (TXA) treatment
Experimental group
Description:
Tranexamic Acid (TXA) treatment
Treatment:
Drug: Tranexamic Acid (TXA) treatment
control grup: without Tranexamic Acid (TXA) treatment.
Experimental group
Description:
control grup: without Tranexamic Acid (TXA) treatment.
Treatment:
Drug: control grup: without Tranexamic Acid (TXA) treatment.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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