Reticulocyte Parameters as Early Indicators of Bone Marrow Erythropoietic Activity in Chronic B Lymphoproliferative Neoplasms
1 other identifier
observational
120
0 countries
N/A
Brief Summary
Reticulocyte parameters as early indicators of bone marrow erythropoietic activity in chronic B lymphoproliferative neoplasms
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 13, 2025
CompletedStudy Start
First participant enrolled
January 1, 2026
CompletedFirst Posted
Study publicly available on registry
January 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2027
January 13, 2026
December 1, 2025
1.1 years
December 13, 2025
January 7, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Reticulocyte count
Absolute peripheral blood reticulocyte count measured in patients with chronic B-cell lymphoproliferative disorders (CLPDs). Unit of Measure: ×10⁹/L
1 year
Reticulocyte percentage
Percentage of reticulocytes among total red blood cells in peripheral blood of patients with CLPDs. Unit of Measure: %
1 year
Immature reticulocyte fraction (IRF)
Proportion of immature reticulocytes in peripheral blood measured in patients with CLPDs. Unit of Measure: %
1 year
Eligibility Criteria
Newly diagnosed adult patients with Chronic B LymphoPoliferative neoplasm according to WHO classification.
You may qualify if:
- \- Newly diagnosed adult patients with Chronic B LymphoPoliferative neoplasm according to WHO classification.
You may not qualify if:
- \) Patients received chemotherapy.
- Patients with Active bleeding
- Patients with recent blood transfusion (less than 2 weeks).
- Patients on haematinics or vitamin B 12 therapy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Resident doctor
Study Record Dates
First Submitted
December 13, 2025
First Posted
January 13, 2026
Study Start
January 1, 2026
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
September 1, 2027
Last Updated
January 13, 2026
Record last verified: 2025-12