The prognostic significance of C-Reactive protein to albumin ratio, albumin to fibrinogen ratio, and serum ferritin level in newly diagnosed de novo Non-M3 acute myeloid leukemia patients
NCT ID NCT07810829
First seen Sep 09, 2026 · Last updated Sep 09, 2026
Summary
This prospective cohort study aims to evaluate the prognostic significance of the C-reactive protein-to-albumin ratio (CAR), albumin-to-fibrinogen ratio (AFR), and serum ferritin level in newly diagnosed de novo non-M3 acute myeloid leukemia patients at Assiut University Hospitals.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 208 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Newly diagnosed de novo non-M3 acute myeloid leukemia patients admitted to the Internal Medicine Department at Assiut University Hospitals.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18 to 65 years * Newly diagnosed de novo non-M3 acute myeloid leukemia * Both sexes * Willingness to provide informed consent Exclusion Criteria: * \- Patient refusal * Significant cardiac, hepatic, or renal disease * Diabetes mellitus with polyneuropathy * Severe organ dysfunction (modified Marshall score ≥ 2) * History of MDS transformed to AML * Previous blood transfusions * Relapsed AML * Previous exposure to chemotherapy or radiotherapy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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