What is the Prognostic Value of HALP Score, Monocytopenia, Hypofibrinogenemia, and AST/ALT Ratio in Patients With Myelodysplastic Syndromes
Prognostic Value of HALP Score, Monocytopenia, Hypofibrinogenemia, and AST/ALT Ratio in Patients With Myelodysplastic Syndromes at Assiut University Hospital.
1 other identifier
observational
100
0 countries
N/A
Brief Summary
to investigate prognostic significance of many factors in MDS including HALP score ( haemoglobin level, albumin level, lymphocyte, platelets), monocytopenia, hyperfibrinogenemia and AST/ALT ratio in patients with MDS at Assiut University Hospital. And to study overall survival and leukemia free survival rates in MDS patients.
Trial Health
Trial Health Score
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participants targeted
Target at P50-P75 for all trials
Started Jan 2026
Typical duration for all trials
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
September 29, 2025
CompletedFirst Posted
Study publicly available on registry
October 7, 2025
CompletedStudy Start
First participant enrolled
January 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2028
October 7, 2025
September 1, 2025
2 years
September 29, 2025
September 29, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
prognostic significance of many factors in MDS
to investigate prognostic significance of many factors in MDS including HALP score ( haemoglobin level, albumin level, lymphocyte, platelets), in patients with MDS at Assiut University Hospital HALP : a derived value from a formula: Hemoglobin (g/L) × Albumin (g/L) × Lymphocytes (/L) / Platelets (/L)
Two years
Eligibility Criteria
Adults (≥18 years old) diagnosed with MDS according to WHO criteria
You may qualify if:
- Adults (≥18 years old) diagnosed with MDS according to WHO criteria
- Availability of complete medical records including laboratory data for hemoglobin, albumin, lymphocyte count, platelet count, monocyte count, fibrinogen level, AST and ALT
- Patients who were followed for at least 12 months post-diagnosis or until death
You may not qualify if:
- Patients with active infections, liver cirrhosis, chronic inflammatory diseases, or concurrent malignancies at time of diagnosis
- Incomplete laboratory or clinical data
- Patients lost to follow-up within less than 3 months of diagnosis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident at internal medicine department
Study Record Dates
First Submitted
September 29, 2025
First Posted
October 7, 2025
Study Start
January 1, 2026
Primary Completion (Estimated)
January 1, 2028
Study Completion (Estimated)
March 1, 2028
Last Updated
October 7, 2025
Record last verified: 2025-09