Replacing Bone Marrow Diagnostics With Peripheral Blood Analysis in Cytopenia Patients
Recruiting now
Conditions studied: Cytopenia, MDS
In brief
This observational, multi-center study aims to collect data in order to develop a novel, minimally invasive diagnostic tool for MDS based on peripheral blood profiling of circulating hematopoietic stem and progenitor cells (cHSPCs) using single-cell RNA sequencing and DNA sequencing.
Key facts
- Study ID
- NCT07081087
- Run by
- Weizmann Institute of Science
- People needed
- 1500
- Starts
- 2025-06-01
- Expected to finish
- 2028-12-01
- Last updated by the study team
- 2026-03-25
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients aged 18 and up with suspected/confirmed MDS cases referred to BM evaluation either for diagnosis or risk assessment due to cytopenia
- Platelets < 150 × 10E9/L or
- Absolute neutrophil count < 1.8 × 10E9/L or
- Hemoglobin (Hgb) < 13 g/dL (males) and < 12 g/dL (female) and
- For both sexes, no evidence of Iron, folinic acid, or B12 deficiency
You may not qualify if…
- Women who are pregnant
- Previous diagnosis of leukemia; AML, MPN, ALL, CLL, MGUS/MM or any other gammopathy
- Lymphocytes > 5000/ul
- Patients who are on disease-related therapy are excluded, unless they are treated with Erythropoietin or Prednisone. See Appendix 2 for the list of excluded treatments.
- Patients who have undergone a bone marrow transplant.
Where it is running
- University of California San Diego — San Diego, California, United States (enrolling)
- University of Miami — Miami, Florida, United States (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.