跳至主要内容
临床试验/NCT06919341
NCT06919341招募中不适用

RESTI Registry: Spanish Registry of Primary Immune Thrombocytopenia and Other Immune Thrombocytopenia

Fundación Española de Hematología y Hemoterapía36 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2024年9月27日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,000
试验地点
36
主要终点
Description of the clinical and analytical features of PIT and other immune thrombocytopenias.

研究概览

简要总结

Primary immune thrombocytopenia (PIT), previously referred to as idiopathic thrombocytopenic purpura, is an acquired disease characterized by accelerated platelet destruction and deficient platelet production by megakaryocytes.

Although the existence of PIT has been known for decades, there is no consensus on its triggering mechanisms. On the other hand, this disease presents a very heterogeneous patient profile, both in its characteristics and treatments. In this sense, the diagnosis is still made by excluding other causes of thrombocytopenia.

There is insufficient epidemiological data on the disease, a fact that is especially evident in our country. We have no data on the incidence or prevalence of this pathology in Spain.

For all these reasons, this epidemiological study has been designed to increase the available knowledge about this disease and the detailed characterization of the population of patients with ITP in Spain.

The main objective of this study is to describe the clinical, analytical and treatment characteristics of primary immune thrombocytopenia and other immune thrombocytopenia.

The study is an epidemiological, ambispective, multicenter study carried out in hospitals in Spain.

Information will be collected on the disease under study, as well as on the treatments received, using the patient's clinical history as a source document.

研究设计

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

入排标准

年龄范围
2 Months 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Children as young as 2 months of age and adults in follow-up since 2015 (irrespective of date of diagnosis) with the diagnostic presumption of PIT or other thrombocytopenia of probable immune origin defined as a platelet count < 100 x 109/L.
  • Patients who have given written informed consent. In the case of deceased patients, the data will be included in the registry and the investigator will record the impossibility of collecting patient's informed consent form due to death. Only patients deceased after December 31 2015, will be included

排除标准

  • Patients who, at the investigator's discretion, do not meet the conditions for inclusion in the study

结局指标

主要结局

Description of the clinical and analytical features of PIT and other immune thrombocytopenias.

时间窗: From enrollment

次要结局

  • Comparison with published historical ITP data(From enrollment)
  • Definition of therapeutic strategies and most common treatments in ITP(From enrollment)
  • Evaluation of response to first-line treatment(From enrollment)
  • Evaluation of response to subsequent treatments(From enrollment)

研究者

发起方
Fundación Española de Hematología y Hemoterapía
申办方类型
Other
责任方
Sponsor

研究点 (36)

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