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临床试验/NCT05641103
NCT05641103已完成不适用

PREDIGA 2: Spanish Acronym of "Educational and Diagnostic Project for Gaucher and ASMD"

Fundación Española de Hematología y Hemoterapía14 个研究点 分布在 1 个国家目标入组 122 人开始时间: 2023年3月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
122
试验地点
14
主要终点
Prevalence of Gaucher disease (GD) and acid sphingomyelinase deficiency (ASMD)

研究概览

简要总结

The study of splenomegaly, and the follow-up of splenectomized patients, is one of the causes of referral of these patients to pediatric gastroenterology and oncohematology clinics, and adult internal medicine and hematology. It has been described that 0.3% of hospital admissions is for this reason.

The study and management of splenomegaly is well described among the different medical specialties to which these patients arrive. After the application of the different algorithms and the different studies that are carried out, these splenomegaly are identified as being of hepatic, infectious, inflammatory, congestive, hematological origin and primary causes. Despite these studies of splenomegaly, approximately 10-15% of these patients still remain undiagnosed.

The objective of the present study is to increase the diagnostic sensitivity of these unknown splenomegalys, or unknown splenomegaly patients who remain in consultations, using the usual diagnostic clinical procedures of unknown splenomegaly and unknown splenectomy patients, where the investigators include the extraction of a blood sample for dry drop test (DBS), where the determination of the enzymatic/genetic activity will be carried out for Gaucher disease (GD) and acid sphingomyelinase deficiency (ASMD) , analysis of LisoGl1 and LisoSM.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients (over 18 years old) of both sexes.
  • Patients presenting signs, assessed instrumentally or via laboratory tests, of:
  • Unexplained splenomegaly, defined as a palpable spleen ≥ 1 cm below the costal margin or diagnosed by ultrasound, magnetic resonance imaging (MRI), or computed tomography (CT) of the spleen.
  • Splenectomized patients without a diagnosis of the cause of unexplained splenomegaly.
  • Patients who provide their consent to participate in the study.

排除标准

  • Splenomegaly due to portal hypertension (documented by abdominal ultrasound or another instrumental test) caused by liver disease
  • Malignant hematologic tumor [documented by positive physical examination + blood smear or fine-needle aspiration (FNA) or bone marrow biopsy]
  • Hemolytic anemia and/or thalassemia
  • Patients unable to comply with the protocol requirements due to psychiatric and/or cognitive disorders, non-cooperative patients, or educational and written language comprehension limitations
  • Patient refusal to participate in the study

结局指标

主要结局

Prevalence of Gaucher disease (GD) and acid sphingomyelinase deficiency (ASMD)

时间窗: 36 months

Determinate the prevalence of Gaucher disease (GD) and acid sphingomyelinase deficiency (ASMD)

次要结局

未报告次要终点

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 (14)

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