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study for the clinician to decide on bone marrow examinatio

Phase 4
Completed
Registration Number
CTRI/2018/03/012407
Lead Sponsor
Patient
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. All cases of thrombocytopenia with platelet count below 1,50,000/cu mm with or without bone marrow studies.

2. The cases with sufficient clinico-haematological work up with established clinical diagnosis will be included.

3. Only one sample of the single participant will be taken.

Exclusion Criteria

1. Pseudothrombocytopenia

2. Patients who have received blood transfusion or platelet transfusion within 7 days

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The cases will be broadly classified into two groups on the basis of cause of thrombocytopenia- due to peripheral hyperdestruction(immune thrombocytopenic purpura; infection like malaria, dengue; drug induced, etc.) and hypoproliferative bone marrow (megaloblastic anaemia; leukaemia; aplastic anaemia; myelodysplastic syndrome; myelofibrosis; multiple myeloma; marrow infilteration).Timepoint: 30th April 2018
Secondary Outcome Measures
NameTimeMethod
Research still going onTimepoint: 31st July 2018
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