首页> 外文期刊>Trials >A feasibility study to inform the design of a randomized controlled trial to identify the most clinically and cost effective Anticoagulation Length with low molecular weight heparin In the treatment of Cancer Associated Thrombosis (ALICAT): study protocol for a mixed-methods study
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A feasibility study to inform the design of a randomized controlled trial to identify the most clinically and cost effective Anticoagulation Length with low molecular weight heparin In the treatment of Cancer Associated Thrombosis (ALICAT): study protocol for a mixed-methods study

机译:一项可行性研究,旨在设计一项随机对照试验,以鉴定最临床和最具成本效益的低分子量肝素抗凝治疗癌症相关血栓形成(ALICAT)的时间:一项混合方法研究的研究方案

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Background Venous thromboembolism is common in patients with cancer and requires anticoagulation with low molecular weight heparin. Current data informs anticoagulation as far as six months, yet guidelines recommend anticoagulation beyond six months in patients who have locally advanced or metastatic cancer. This recommendation, based on expert consensus, has not been evaluated in a clinical study. ALICAT (Anticoagulation Length in Cancer Associated Thrombosis) is a feasibility study to identify the most clinically and cost effective length of anticoagulation with low molecular weight heparin in the treatment of cancer associated thrombosis. Methods/Design ALICAT is a randomized multi-centre phase two mixed-methods study with three components: a randomized controlled trial, embedded qualitative study and a survey investigating pathways of care. The randomized controlled trial will compare ongoing low molecular weight heparin treatment for cancer-associated thrombosis versus cessation of low molecular weight heparin at six months treatment (current licensed practice) in patients with locally advanced or metastatic cancer. The embedded qualitative study will include focus groups with clinicians to investigate attitudes to recruiting to the study, identify the challenges of progressing to a full randomized controlled trial, and also semi-structured interviews with patients and relatives/carers to explore their attitudes towards participating in the study and potential barriers and concerns to participation. Finally, a UK wide survey exercise will be undertaken to develop a classification and enumeration system for the cancer associated thrombosis models and pathways of care. Discussion There is a lack of evidence determining the length of anticoagulation for patients with cancer associated thrombosis and subsequently treatment length varies. The ALICAT study will consider the feasibility of recruiting patients to a phase three trial. Trial registration Current Controlled Trials ISRCTN37913976 .
机译:背景技术静脉血栓栓塞症在癌症患者中很常见,需要使用低分子量肝素进行抗凝治疗。目前的数据可告知抗凝治疗长达六个月,但指南建议局部晚期或转移性癌症患者抗凝治疗应超过六个月。基于专家共识的此建议尚未在临床研究中进行评估。 ALICAT(癌症相关血栓形成中的抗凝长度)是一项可行性研究,旨在确定低分子量肝素在治疗癌症相关血栓形成中最临床和最具成本效益的抗凝长度。方法/设计ALICAT是一项多中心随机,两阶段混合方法研究,包含三个组成部分:随机对照试验,嵌入式定性研究和调查研究途径。该随机对照试验将比较正在进行的低分子量肝素治疗与癌症相关的血栓形成与在局部晚期或转移性癌症患者中治疗六个月(目前许可的实践)低分子量肝素停止治疗的比较。嵌入式定性研究将包括与临床医生的焦点小组,以调查招募该研究的态度,确定进行完全随机对照试验的挑战,以及对患者和亲戚/护理人员的半结构化访谈,以探讨他们对参与研究的态度研究,参与的潜在障碍和关注。最后,将进行英国范围的调查,以开发与癌症相关的血栓形成模型和护理途径的分类和枚举系统。讨论尚无证据确定癌症相关血栓形成患者的抗凝时间长短,随后的治疗时间长短不一。 ALICAT研究将考虑招募患者参加第三阶段试验的可行性。试用注册电流控制试验ISRCTN37913976。

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