Clinical, Hematological and Pathological Profile of Pancytopenia

ConditionPancytopenia
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorAssiut University

About this trial

Describe clinical characteristic, peripheral blood parameters and bone marrow examination in pancytopenia patients and Analyze etiology of pancytopenia and study the outcomes regarding duration of hospital stay.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

The study population consists of patients of different age groups and both sexes who present with clinical manifestations and laboratory findings suggestive of pancytopenia, attending the inpatient departments or outpatient clinics at Assiut University Hospitals.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

140 Participants
are grouped into 1 trial group
Group A: Pancytopenia Cases

Trial outcomes

Primary outcomes

1

Proportion of underlying etiologies of pancytopenia

Percentage of study participants diagnosed with each etiology of pancytopenia based on clinical, hematological, and pathological evaluation

Time frame
At the time of patient enrollment and initial diagnostic workup

Secondary outcomes

1

Frequency of clinical features and hematological parameters in pancytopenia patients

Percentage of patients presenting with specific clinical symptoms (e.g., pallor, bleeding, fever) and distribution of CBC findings (e.g., hemoglobin levels, absolute neutrophil count, platelet count).

Time frame
At baseline
2

Distribution of bone marrow pathological findings

Percentage of patients categorized by bone marrow aspirate and biopsy findings (e.g., hypercellular, hypocellular, dysplastic changes )

Time frame
At baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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