Transfusion in Lower Risk MDS Patients: Predictors of Adequacy of Transfusion and Quality of Life in Lower Risk MDS

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFundación para la Investigación Biosanitaria del Principado de Asturias

About this trial

Observational study to evaluate changes in quality of life (QoL) in patients diagnosed with low risk MDS who are red blood cell (abc) transfusion dependent.

Changes in QoL will be correlated with patient cardiorespiratory function. Cardiac biomarkers and plasma cytokines will also be evaluated.

Eligibility criteria

Qualifiers

They must be able to understand the study procedures, comply with them, and consent in writing prior to any specific study procedure.

Must be able to understand the study procedures, comply with them, and give written informed consent prior to any study-specific procedure.

Adult subjects ≥ 18 years of age with a diagnosis of myelodysplastic syndrome.

Very low, low or intermediate IPSS-R risk category.

Disqualifiers

Subject undergoing any of the following treatments: azacitidine, decitabine, venetoclax, cytotoxic chemotherapy, radiotherapy, arsenic trioxide, interferon or interleukin.

High or very high IPSS-R risk category.

epidermoid or basal cell carcinoma,

carcinoma in situ of the uterine cervix

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators