跳至主要内容
临床试验/EUCTR2005-005957-23-IT
EUCTR2005-005957-23-IT进行中(未招募)不适用

RANDOMIZED CLINICAL STUDY OF DIFFERENT DOSES And DURATION OF PARNAPARINA In the TREATMENT Of SUPERFICIAL VENOUS THROMBOSIS - STEFLUX STUDY - STEFLUX

AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI0 个研究点目标入组 900 人开始时间: 2006年3月15日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
900

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Age 18 years weight 50 kg and inferior to 110 kg TVS of the large v. safena extended in order at least 5 cm TVS of the small v. safena extended in order at least 5 cm collaterals TVS of large v. safena in the thigh extended in order at least 5 cm
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Age 85 years TVS of large saphena that catches up the zone from the safeno-femoral cross or for which it is indicated the oral anticoagulating therapy or the cross safeno-femoral ligature TVS of the small saphena that catches up the cross safeno-poplitea or for which it is indicated the oral anticoagulating therapy Documented proximal TVP or distal TVP or pulmonary embolism Secondary TVS to sclerotherapy Pregnancy and puerperium Arterial hypertension not controlled systolic 180 mmHg and diastolic PA 110 mmHg Active or past peptic ulcer Bacterial endocarditis Ictus in the previous 3 months haemorrhagic diathesis Piastrinopenia platelet 100,000/ L Hypersensitivity to heparin or induced history of piastrinopenia from heparin Creatininemia 2 mg 180 mol/L Contraindications to elastic stockings or compressivo handwraps Anticoagulating or heparinic therapy in the previous 72 hours Active cancer or chemotherapeutic or radiotherapeutic treatment Refusal of the informed consent

研究者

发起方
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI

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