Fact CheckerSign in

NCT06794281Active, not recruiting

Synthetic Generation of Hematological Data Over Federated Computing Frameworks: SCD Use Case

Synthetic Generation of Hematological Data Over Federated Computing Frameworks (SYNTHEMA): SCD Use Case

Source: ClinicalTrials.gov · Last updated 12 Mar 2025

Brief summary (registry, in English)

Haematological diseases (HDs) are a large group of disorders resulting from quantitative or qualitative abnormalities of blood cells, lymphoid organs and coagulation factors. Despite most of them (\~74%) are rare, the overall number of HD affected patients worldwide is important, placing a considerable economic burden on healthcare systems and societies. Despite the existence of several collaborative research groups at national and EU level, current clinical approaches are often ineffective, particularly for rarest conditions, due to the relatively low number of patients per disease and the high number of unconnected clinical entities. SYNTHEMA aims to establish a cross-border data hub where to develop and validate innovative AI-based techniques for clinical data anonymisation and synthetic data generation (SDG), to tackle the scarcity and fragmentation of data and widen the basis for GDPR-compliant research in rare hematological disorders (RHD). The project will focus on one representative RHD use case: sickle-cell disease (SCD).

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
1500 (estimated)
First submitted
21 Jan 2025
Start date
1 Nov 2022
Primary completion date
30 Nov 2026
Lead sponsor
Hospital Universitari Vall d'Hebron Research Institute
NCT number
NCT06794281

What you commit to

  • Study type: Observational
  • Planned participants: 1500
  • From 1 Nov 2022 to the primary completion date, 30 Nov 2026
  • 3 sites in 3 countries
  • 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.

Age

  • younger than 1 year old

Other

  • post HSCT patients

Who the study is looking for

  • SCD patients (any genotype).
  • older than 1 year old

Age in the registry: 1 year to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

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

SiteCityCountrySite status
Vall Hebron Institut de Recerca
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Azienda Ospedale Universita Padova
Coordinator of this site? Confirm its status
PadovaItalyUnknown status
UMC Utrecht
Coordinator of this site? Confirm its status
UtrechtNetherlandsUnknown status

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