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临床试验/NCT06393868
NCT06393868招募中3 期

Reducing Gastrointestinal Bleeding With Proton Pump Inhibitor Therapy in Acute Venous Thromboembolism: Pilot Randomized Study (RADIANT Study)

Ottawa Hospital Research Institute9 个研究点 分布在 1 个国家目标入组 360 人开始时间: 2024年11月6日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
招募中
入组人数
360
试验地点
9
主要终点
Study feasibility at participating centres

研究概览

简要总结

The investigators are studying whether treatment with a proton pump inhibitor called omeprazole reduces gastrointestinal bleeding in older adults taking blood thinners for a blood clot (venous thromboembolism). The purpose of this study, a pilot study or a feasibility study, is to test the study plan and determine whether enough participants will join a larger study and accept the study procedures.

详细描述

Venous thromboembolism (VTE) refers to blood clots that form in the veins of the body, including the arms or legs (deep vein thrombosis [DVT]), abdomen (portal vein thrombosis), or lungs (pulmonary embolism [PE]). These blood clots are treated with medication to reduce blood clotting called anticoagulants. The main complication of anticoagulants is bleeding, the majority of which comes from the stomach or intestines (gastrointestinal tract). Anticoagulants do not cause bleeding, but they may make bleeding worse. Uncommonly, serious gastrointestinal (GI) bleeding can happen leading to hospitalization and even death. The chance of bleeding is highest in the first few months after starting anticoagulants.

Proton pump inhibitors (PPIs) are medications that lower the acid content of the stomach. The medication in this study, a type of proton pump inhibitor called omeprazole, is approved in Canada for treating stomach ulcers, heartburn, and a stomach infection called Helicobacter pylori. The use of omeprazole in this study is considered investigational. This means that Health Canada has not approved the use of omeprazole as a treatment for preventing gastrointestinal bleeding in patients taking anticoagulants. Some studies suggest that they may reduce gastrointestinal bleeding for people taking anticoagulants.

The investigators are studying whether treatment with a proton pump inhibitor called omeprazole reduces gastrointestinal bleeding in older adults taking anticoagulants for venous thromboembolism.

The investigators plan to do a large, randomized trial which is the best way to test the effect of a treatment. To do this, some of the participants in this study will get omeprazole and others will get a placebo (a substance that looks like the study omeprazole but does not have any active or medicinal ingredients). The placebo in this study is not intended to have any effect on bleeding. A placebo is used to make the results of the study more reliable.

Primary Objective To assess the feasibility of a full-scale double-blind placebo-controlled randomized trial to determine whether omeprazole reduces the risk of upper GI bleeding in older adults receiving anticoagulation for acute VTE compared to placebo.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Male or female 65 years or older at the time of enrolment. Enrolment is limited to older adults as age is an important non-modifiable risk factor for bleeding. This will ensure the study population includes participants who may be more likely to benefit from omeprazole (compared to those with no risk factors) because all participants will have at least 1 risk factor for bleeding.
  • Newly diagnosed VTE which includes VTE at any site such as (but not limited to) DVT of upper or lower limbs, PE, cerebral vein thrombosis, portal vein thrombosis, other splanchnic vein thrombosis.
  • Planned for 3 months (90 days) or more of therapeutic anticoagulation with any anticoagulant.
  • Patient or delegate is able and willing to comply with follow-up examinations contained within the consent form.

排除标准

  • Therapeutic anticoagulation therapy for more than 7 days
  • Currently prescribed PPI for regular daily use (patients receiving H2 receptor antagonists will not be excluded),
  • Previous upper GI bleeding,
  • Need for dual antiplatelet therapy,
  • Contraindications to omeprazole (hypersensitivity to omeprazole, or other substituted benzimidazole PPIs, concomitant use with products that contain rilpivirine, significant drug interactions, up to the discretion of the site investigator),
  • Life expectancy is less than 3 months.

研究组 & 干预措施

Daily dose of placebo

Placebo Comparator

Participants randomized to the control arm will take one placebo tablet by mouth every day for the duration of their participation in the study.

干预措施: Placebo (Other)

Daily dose of omeprazole 20 mg

Experimental

Participants randomized to the experimental arm will take one omeprazole 20 mg tablet by mouth every day for the duration of their participation in the study.

干预措施: Omeprazole 20 mg Oral Tablet (Drug)

结局指标

主要结局

Study feasibility at participating centres

时间窗: 24 months

The mean number of participants recruited per site per month

次要结局

  • Adherence Rate(27 months)
  • Eligibility Rate(24 months)
  • Consent Rate(24 months)
  • Retention Rate(27 months)

研究者

申办方类型
Other
责任方
Sponsor
主要研究者

Deborah Siegal

Qualified Investigator

Ottawa Hospital Research Institute

研究点 (9)

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