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临床试验/NCT01034488
NCT01034488Unknown2 期

Pharmacodynamics Aspects Of Porcine Heparin Sodium, Produced by Eurofarma, Compared Heparin Sodium, Produced by APP Pharmaceuticasls, in Patients With Chronic Renal Failure

Azidus Brasil0 个研究点目标入组 128 人开始时间: 2010年8月最近更新:
适应症

试验速览

阶段
2 期
发起方
Azidus Brasil
入组人数
128
主要终点
Effect (activity) of heparin observed for markers for aPTT and anti-Xa.

研究概览

简要总结

  1. Background: Heparin forms a complex with a plasma protein, antithrombin III (ATIII) is an endogenous anticoagulant. This complex inhibits the formation of thrombin and accelerates its destruction. In addition, heparin and ATIII inactivate other proteases of the coagulation cascade, especially the anti-activated factor X. The outcome of these biochemical actions is the inhibition of the formation and synthesis of activators of the clotting factors that exert critical functions in the genesis of the blood clot. Patients with chronic renal failure (CRF) that make use of hemodialysis need a system of anticoagulation with direct inhibitors of thrombin and / or heparinoids to prevent thrombosis.

Based on clinical studies, the control of plasma heparin level in patients with CRF is essential. Coagulation tests such as APTT, PT, ChT and evidence of activity of anti-Xa factor to be used as a substrate for protection for those patients undergoing hemodialysis. 2. Objective: Check the non-inferiority clinical, the pharmacodynamic effect and safety in use of the drug heparin of porcine origin, produced by the Laboratory Eurofarma, having as the active comparator drug APP ® Heparin Sodium (heparin - APP Pharmaceuticals) in patients with renal failure who do hemodialysis treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults of both sexes, regardless of color or social class;
  • Age over 18 years, with good clinical doctor's discretion;
  • Patients research that agree to participate in the study and sign the informed consent form (attached);
  • Chronic renal failure patients in hemodialysis (3 times per week). chronic renal failure patients with indication for anticoagulation during dialysis

排除标准

  • Non compliance with the terms described in the informed consent FICT;
  • Patients suffering from sensitivity studies heparin sodium;
  • Patients with hypersensitivity to search benzyl alcohol;
  • Patients with search history of bleeding disorders or disease that a bleeding disorder can worsen or terminate the clinical picture, for example, frames of gastric ulcer;
  • Patients with a history of research peptic ulcer;
  • Patient with cancer research because of the possibility of impairment of variable coagulation function;
  • Patients who are research during pregnancy and postpartum;
  • Individuals with a genetic abnormality of the coagulation system;
  • Trauma patients;
  • Patients on glucocorticoid therapy for at least 1 month;
  • Patients using other anticoagulants;
  • Patients with a high rate of bleeding;
  • Patients undergoing any surgery performed less than 15 days due to the risk of bruising at the site of surgery.
  • Patients using drugs that affect hemostasis
  • Patients using the following drugs: Salicylates systemic aspirin and other NSAIDs, including ketorolac, Dextran 40, ticlopidine and clopidogrel, systemic glucocorticoids, thrombolytic agents and anticoagulants and other antiplatelet agents, including antagonists of glycoprotein IIb / IIIa.

结局指标

主要结局

Effect (activity) of heparin observed for markers for aPTT and anti-Xa.

时间窗: 12 hemodialysis sessions in a row. The sessions take place 3 times a week. So be 4 weeks.

次要结局

  • Effectiveness in maintaining the absence clotting during hemodialysis.(12 consecutive sessions)
  • Safety in use of the drug by monitoring events complicating the use of heparin(12 consecutive sessions)

研究者

发起方
Azidus Brasil
申办方类型
Industry

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