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NCT05992532Recruiting

GammaGA: Prevalence of Acid Sphingomyelinase Deficiency Disease (ASMD) and Gaucher Disease in Patients With Monoclonal Gammopathies and/or Multiple Myeloma

GammaGA: Study of the Prevalence of Acid Sphingomyelinase Deficiency Disease (ASMD) and Gaucher Disease in Patients With Monoclonal Gammopathies and/or Multiple Myeloma

Source: ClinicalTrials.gov · Last updated 11 Feb 2026

Brief summary (registry, in English)

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. 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. Several studies have suggested that there is an increased frequency of MGUS (monoclonal gammopathy of undetermined significance) and/or multiple myeloma (MM) among Gaucher patients. Regarding ASMD (Acid Sphingomyelinase Deficiency), few studies have been published but it seems the 21% of patient with ASMD has MGUS and 15% ASMD patients have MGUS. Moreover, patients with MGUS and Gaucher disease (GD) are at increased risk of developing MM. The objective of the present study is to increase the diagnostic sensitivity of these unknown splenomegalys, or unknown splenomegaly patients with MGUS or multiple myeoloma who remain in consultations, using the usual diagnostic clinical procedures of unknown splenomegaly and unknown splenectomy patients, where we 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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
210 (estimated)
First submitted
8 Aug 2023
Start date
30 May 2023
Primary completion date
31 Dec 2025
Lead sponsor
Fundación Española de Hematología y Hemoterapía
NCT number
NCT05992532

What you commit to

  • Study type: Observational
  • Planned participants: 210
  • From 30 May 2023 to the primary completion date, 31 Dec 2025
  • 23 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Splenomegaly due to portal hypertension (documented by abdominal ultrasound or other instrumental test) due to liver disease
  • Hematologic malignancy \[documented by positive physical exam + blood smear or fine needle aspiration (FNA) or bone marrow biopsy\]

Other

  • Hemolytic anemia and/or thalassemia
  • Patients who cannot meet the requirements of the protocol due to mental and/or cognitive alterations, uncooperative patients, educational limitations and understanding of written language
  • Refusal of the patient to participate in the study

Who the study is looking for

  • Adult patients of both sexes.
  • Patients with splenomegaly (spleen palpable at ≥ 1cm from the costal margin) or splenectomy not related to any specific condition, or patients with thrombocytopenia (with or without splenomegaly). In cases where the patient is undergoing treatment for their underlying condition, the thrombocytopenia must have been present prior to the start of the treatment.
  • Patient who gives their consent to participate in the study.

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (23)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital Alcañiz
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AlcañizSpainRecruiting
Hospital Universitario Torrecárdenas
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AlmeríaSpainRecruiting
Complejo Asistencial de Ávila
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ÁvilaSpainRecruiting
Hospital Universitario De Burgos
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BurgosSpainRecruiting
Hospital Universitario Dr. Josep Trueta
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GironaSpainRecruiting
Hospital Universitario Virgen de las Nieves
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GranadaSpainRecruiting
Hospital San Jorge
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HuescaSpainRecruiting
Hospital de Jaen
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JaénSpainRecruiting
Hospital Arnau de Vilanova
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LleidaSpainRecruiting
Hospital Fundación Jimenez Diaz
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MadridSpainRecruiting
Hospital Universitario La Paz
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MadridSpainRecruiting
Hospital Universitario Ramón y Cajal
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MadridSpainRecruiting
Hospital Regional Universitario de Malaga
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MálagaSpainRecruiting
Complejo Hospitalario Universitario de Orense
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OurenseSpainRecruiting
Hospital Son Espases
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Palma de MallorcaSpainRecruiting
Hospital del Bierzo
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PonferradaSpainRecruiting
Hospital Parc Tauli
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SabadellSpainRecruiting
Hospital de Valdepeñas
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ValdepeñasSpainRecruiting
Hospital de Manises
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ValenciaSpainRecruiting
Hospital Universitario Y Politecnico La Fe
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ValenciaSpainRecruiting
Hospital Clínico Universitario de Valladolid
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ValladolidSpainRecruiting
Hospital Alvaro Cunqueiro
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VigoSpainRecruiting
Hospital Universitario de Álava
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Vitoria-GasteizSpainRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.