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临床试验/NCT04994223
NCT04994223Unknown早期 1 期

Effectiveness of Combined Anticoagulation and Antithrombotic Therapy vs Antithrombotic Therapy Alone After Lower Extremity Revascularization for Peripheral Arterial Disease

Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年7月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
发起方
入组人数
60
试验地点
1
主要终点
ALI

研究概览

简要总结

EFFECTIVENESS OF COMBINED ANTICOAGULATION AND ANTITHROMBOTIC THERAPY VS ANTITHROMBOTIC THERAPY ALONE AFTER LOWER EXTREMITY REVASCULARIZATION FOR PERIPHERAL ARTERIAL DISEASE.

详细描述

Anticoagulation and antithrombotic therapy is a crucial part of PAD management as it prolongs the patecy of grafts in open surgical revascularization procedures so its proper dosage and duration without increasing risks to the patient and maximizing the benefits is very important.

Currently literature in Pakistan regarding this problem couldn't be found so this study would help assessing the outcomes of anticoagulation and antithrombotic therapy in this population with respect to treatment options available and presentation variability of the peripheral arterial disease. Patients with PAD would be enrolled for 6 months and would be followed upto 12 months and then upto 24 months.

Eligible subjects will be randomized 1:1 to receive either rivaroxaban 5 mg twice daily plus aspirin 75 mg once daily or rivaroxaban-matching placebo twice daily plus aspirin 75 mg once daily stratified by type of procedure; the treatment assignment will be double-blinded. Randomization and study treatment will begin as soon as possible but no later than 10 days after a successfull lower extremity revascularization.

Patients will be prohibited from taking any additional antithrombotic therapy other drugs, including anticoagulants, doses of aspirin >100 mg daily, vorapaxar, ticagrelor, prasugrel, or cilostazol. Enrolled subjects will be having symptomatic PAD defined by evidence of an abnormal ankle-brachial index ≤0.80 in either limb with an anatomy of occlusive disease of involving segments. Subjects would be randomized who had undergone a technically successful endovascular, hybrid, or surgical LER within 10 days and had achieved adequate hemostasis before randomization.

研究设计

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

盲法说明

participants enrolled in the study and the principal investigator would not be knowing the drug regimens used in group A and Group B participants

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • all patients with PAD candidates for revascularization procedures

排除标准

  • planned long-term dual antiplatelet therapy (>6 months),
  • clinical requirement for therapeutic anticoagulation,
  • recent acute limb ischemia or acute coronary syndrome,
  • medical condition that could increase the risk of major bleeding, significantly impaired renal function at baseline (estimated glomerular filtration rate <15 mL•min-1•1.73 m-2),
  • any documented history of intracranial hemorrhage, stroke, or transient ischemic attack

研究组 & 干预措施

Group A(combined anticoagulation plus antithrombotic therapy group)

Experimental

group A patients would be receiving rivaroxaban and aspirin as experimental group to see the efficacy of rivaroxaban in peripheral arterial disease.

干预措施: Rivaroxaban 10 MG Oral Tablet [Xarelto] (Drug)

Group B( antithrombotic therapy alone group)

Active Comparator

group B patients would be those receiving traditional antithrombotic therapy as usually given n Peripheral Arterial Disease.

干预措施: Rivaroxaban 10 MG Oral Tablet [Xarelto] (Drug)

结局指标

主要结局

ALI

时间窗: upto 1 year

acute limb ischemia

major amputation for vascular reasons

时间窗: upto 1 year

any type of major amputation after revascularivation for PAD

MI

时间窗: upto 1 year

myocardial infarction

ischemic stroke

时间窗: upto 1 year

ischemic stroke

cardiovascular death

时间窗: upto 1 year

death because of cardiovascular events

次要结局

  • thrombolysis in myocardial infarction(TIMI)major bleeding(2, 30, 180 and 365 days)

研究者

发起方
Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ayesha Masood

Trainee in vascular surgery

Armed Forces Post Graduate Medical Institute (AFPGMI), Rawalpindi

研究点 (1)

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