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临床试验/NCT01959555
NCT01959555已完成不适用

Project to Update the Study of Congenital Haemophilia in Spain

Novo Nordisk A/S0 个研究点目标入组 1,157 人开始时间: 2014年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,157
主要终点
Severity (mild, moderate or severe) of congenital haemophilia A and B in Spain during 2013, described as proportion (%) per category of the total number of patients with haemophilia A or B

研究概览

简要总结

This study is conducted in Europe. The aim of the study is to update the knowledge about the prevalence and severity of congenital haemophilia (A and B) in Spain.

研究设计

研究类型
Observational
时间视角
Retrospective

入排标准

性别
Male
接受健康志愿者

入选标准

  • Informed consent obtained before any study-related activities. (Study-related activities are any procedure related to recording of data according to the protocol)
  • Male patients of any age diagnosed with congenital haemophilia A or B who visited their HTC at least once during the period of January 2013 to December 2013

排除标准

  • Previous participation in this study
  • Female patients
  • Acquired haemophilia

结局指标

主要结局

Severity (mild, moderate or severe) of congenital haemophilia A and B in Spain during 2013, described as proportion (%) per category of the total number of patients with haemophilia A or B

时间窗: Assessed at study visit (day 1)

Prevalence of congenital haemophilia A and B in Spain in 2013, described as proportion (%) of patients in the total population (extracted from the last available census of the Spanish population for the regions considered for the study)

时间窗: Assessed at study visit (day 1)

次要结局

  • Mean current age at the time of visit to the HTC in 2013(Assessed at study visit (day 1))
  • Proportion (%) of patients with/without genetic screening performed(Assessed at study visit (day 1))
  • Proportion (%) of patients who received on demand or prophylaxis treatment(Assessed at study visit (day 1))
  • Proportion (%) of patients with HIV (Human immunodeficiency virus)(Assessed at study visit (day 1))
  • Proportion (%) of patients with presence of inhibitors(Assessed at study visit (day 1))
  • Proportion (%) of patients with immune tolerance induction treatment performed(Assessed at study visit (day 1))
  • Total number of surgery interventions performed(ThAssessed at study visit (day 1))
  • Mean number of days of absenteeism from work in 2013(Assessed at study visit (day 1))
  • Proportion (%) of patients who needed support of a reference Haemophilia Healthcare Centre in 2013(Assessed at study visit (day 1))
  • Proportion (%) of patients who received plasmatic or recombinant treatment(Assessed at study visit (day 1))
  • Mean number of bleeding episodes(Assessed at study visit (day 1))
  • Mean number of joint bleeds(Assessed at study visit (day 1))
  • Proportion (%) of patients with infectious complications(Assessed at study visit (day 1))
  • Proportion (%) of patients with quality of life questionnaire (QoLQ) performed in 2013(Assessed at study visit (day 1))
  • Mean number of days of absenteeism to school/university in children and adolescents in 2013(Assessed at study visit (day 1))
  • Proportion (%) of patients with treatment administered at home(Assessed at study visit (day 1))
  • Mean age at diagnosis(Assessed at study visit (day 1))
  • Proportion (%) of patients with established arthropathy(Assessed at study visit (day 1))

研究者

申办方类型
Industry
责任方
Sponsor

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