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NCT Number: NCT07337967

Reticulocyte Parameters as Early Indicators of Bone Marrow Erythropoietic Activity in Chronic B Lymphoproliferative Neoplasms

Reticulocyte parameters as early indicators of bone marrow erythropoietic activity in chronic B lymphoproliferative neoplasms

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Newly diagnosed adult patients with Chronic B LymphoPoliferative neoplasm according to WHO classification.

Exclusion criteria

  • Patients received chemotherapy.
  • Patients with Active bleeding
  • Patients with recent blood transfusion (less than 2 weeks).
  • Patients on haematinics or vitamin B 12 therapy

Treatment and study plan

Primary outcomes

  1. Reticulocyte count

    Time frame: 1 year

    Absolute peripheral blood reticulocyte count measured in patients with chronic B-cell lymphoproliferative disorders (CLPDs).

    Unit of Measure: ×10⁹/L

  2. Reticulocyte percentage

    Time frame: 1 year

    Percentage of reticulocytes among total red blood cells in peripheral blood of patients with CLPDs.

    Unit of Measure: %

  3. Immature reticulocyte fraction (IRF)

    Time frame: 1 year

    Proportion of immature reticulocytes in peripheral blood measured in patients with CLPDs.

    Unit of Measure: %

Sponsors and collaborators

Lead sponsor

Huda Ahmed Abdelsabour Abdelwahab

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jan 13, 2026
Registry last updated
Jan 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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