RECRUITING

Replacing Bone Marrow With Peripheral Blood in Cytopenia Patients

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study aims to validate a novel, non-invasive diagnostic approach for blood and bone marrow malignancies using single-cell RNA sequencing of circulating hematopoietic stem and progenitor cells (cHSPCs) from peripheral blood. Building on prior work defining normal cHSPC profiles in healthy individuals, the study introduces a pipeline for identifying blood pathologies, with a focus on improving the diagnosis and subclassification of myelodysplastic syndromes (MDS). A multi-center clinical trial is proposed to evaluate the method's ability to predict bone marrow results in patients with cytopenia, potentially reducing reliance on bone marrow biopsies.

Official Title

Multi-Center Clinical Trial to Replace BM Analysis of Cytopenia by a Peripheral Blood Assay

Quick Facts

Study Start:2025-06-01
Study Completion:2028-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07081087

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Platelets \< 150 × 109/L or
  2. * Absolute neutrophil count \< 1.8 × 109/L or
  3. * Hemoglobin (Hgb) \< 13 g/dL (males) and \< 12 g/dL (female) and
  4. * For all genders, no evidence of Iron, folinic acid, or B12 deficiency
  5. * All subjects should be referred for BM analysis
  1. * Previous diagnosis of leukemia (AML, MPN, ALL, CLL, MGUS/MM or any other gammopathy)
  2. * Lymphocytes\>5000/ul
  3. * If patients are recruited after
  4. * Diagnosis of any disease related therapy 3 month prior to enrollment

Contacts and Locations

Study Contact

Clinical Trial Manage
CONTACT
+972522666230
gil.gonen-yaacovi@weizmann.ac.il
Liran Shlush, Prof.
CONTACT
+972505109815
liran.shlush@weizmann.ac.il

Study Locations (Sites)

University of Miami
Miami, Florida, 33146
United States

Collaborators and Investigators

Sponsor: Weizmann Institute of Science

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-06-01
Study Completion Date2028-12

Study Record Updates

Study Start Date2025-06-01
Study Completion Date2028-12

Terms related to this study

Additional Relevant MeSH Terms

  • Cytopenia