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临床试验/NCT02502409
NCT02502409Unknown不适用

Natural History Study of Factor IX Treatment and Complications

Skane University Hospital1 个研究点 分布在 1 个国家目标入组 550 人开始时间: 2015年7月最近更新:
适应症

试验速览

阶段
不适用
入组人数
550
试验地点
1
主要终点
Inhibitory antibodies

研究概览

简要总结

This study will examine two groups of subjects with factor IX (FIX) deficiency: 1) those with a current or history of inhibitors to FIX, and; 2) groups of two or more affected brothers, with or without inhibitors. The overall goal is to characterize the study groups in terms of their medical history, their patterns of bleeding, their care, quality of life, and complications including the development of joint disease, inhibitory antibodies to FIX, use of immune tolerance induction (ITI) and outcome.

详细描述

Hemophilia B, FIX deficiency, is the second most common type of hemophilia, occurring in about one in 25,000 male births. This disease is in some ways more complex than hemophilia A, and is less well understood. Differences include a lower incidence and a greater risk of side effects to treatment, for example, allergic reactions and kidney disease. This study will examine two groups of subjects with FIX deficiency - those with a current or history of inhibitors to FIX, and groups of two or more affected brothers, with or without inhibitors. The overall goal is to characterize the study group in terms of their medical history, their patterns of bleeding, their care, quality of life, and complications including the development of inhibitory antibodies to FIX, allergies, kidney, and joint disease.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • A consent approved by the appropriate Institutional Review Board (IRB)/Independent Ethics Committee (IEC) has been obtained from the subject or his legally acceptable representative
  • Subject has FIX deficiency AND
  • Is part of an affected brother pair/group that will also enroll; AND/OR
  • Has a current or history of inhibitor, defined as >0.6 Bethesda units (BU)

排除标准

  • Subject has another congenital bleeding disorder
  • Subject is a carrier of hemophilia B with factor level >0.40 IU/mL

结局指标

主要结局

Inhibitory antibodies

时间窗: Baseline

Current or history of inhibitors

Hemophilia treatment adherence

时间窗: Baseline

Validated Hemophilia Regimen Treatment Adherence Scale--Prophylaxis (VERITAS-Pro), Validated Hemophilia Regimen Treatment Adherence Scale - PRN (VERITAS-PRN)

Annualized bleeding rate

时间窗: 6 months

Overall and by bleeding site

Joint assessment

时间窗: Baseline

Range of motion

Renal disorders

时间窗: 6 months

Reported subject and family history of renal disease

Non-inhibitory antibodies

时间窗: Baseline

Measured at central laboratory

Health related quality of life

时间窗: Baseline

European Quality of Life - 5 Dimensions (EQ5D)

次要结局

  • number of days missed from school or work(6 months)
  • Factor IX usage(6 months)
  • Number of hospitalizations(6 months)
  • Number of surgical procedures(6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sharyne M. Donfield, Ph.D.

Principal Investigator, Data Coordinating Center, Rho, Inc.

Skane University Hospital

研究点 (1)

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