Status:

SUSPENDED

Safe Use of Heparin Sodium in Patients With Chronic Renal Failure.

Lead Sponsor:

Azidus Brasil

Conditions:

Chronic Renal Failure

Eligibility:

All Genders

18+ years

Phase:

PHASE2

PHASE3

Brief Summary

The Heparin form a complex with a plasma protein, antithrombin III (ATIII), which is an endogenous anticoagulant. This complex inhibits the formation of thrombin and accelerates its destruction. Moreo...

Eligibility Criteria

Inclusion

  • Adults of both sexes, regardless of color or social class;
  • Age above 18 years;
  • Patients who agree to participate in the study and signed the free and informed consent (attached);
  • Insufficient patients in chronic renal dialysis scheme (3 times per week);
  • Low Chronic Renal indication of anticoagulant during dialysis.

Exclusion

  • Not agree to the terms described in informed consent;
  • Patients with sensitivity to heparin sodium;
  • Volunteer search with hypersensitivity to benzyl alcohol;
  • Patients with a history of bleeding or change in blood clotting that can aggravate or terminate the clinical picture, such as tables of gastric ulcer;
  • Patients with a history of peptic ulcer;
  • Patients with cancer of any etiology, because of the possibility of compromising the function of the variable coagulation;
  • Patients in a period of pregnancy and postpartum;
  • Individuals with genetic abnormality of clotting system;
  • Patients polytraumatized;
  • Patients in use of glucocorticoids for at least 1 month;
  • Patients in use of other anticoagulants;
  • Patients with high rate of bleeding;
  • Patients undergo any surgery performed less than 15 days because of the risk of the formation of hematomas at the site of surgery;
  • Patients in use of drugs that affect the hemostasis;
  • In addition to these, clinical characteristics that the medical criteria, can interfere with the study.

Key Trial Info

Start Date :

July 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

July 1 2008

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT01229072

Start Date

July 1 2008

End Date

July 1 2008

Last Update

November 3 2022

Active Locations (1)

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Lal Clinica Pesquisa E Desenvolvimento Ltda

Valinhos, São Paulo, Brazil, 13270000