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Clinical Trials/NCT01680055
NCT01680055
Withdrawn
Not Applicable

Collection of Blood and Bone Marrow From Patients With Aplastic Anemia for Analysis of Adhesion Molecules, Chemokines and Their Receptors

Shandong University1 site in 1 countryFebruary 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aplastic Anemia
Sponsor
Shandong University
Locations
1
Primary Endpoint
hematologic response
Status
Withdrawn
Last Updated
10 years ago

Overview

Brief Summary

This study is designed to collect bone marrow and/or peripheral blood cells and plasma, for the analysis of adhesion molecules, chemokines and their receptors from newly-diagnosed aplastic anemia patients, and patients treated with antithymocyte globulin plus cyclosporine

Registry
clinicaltrials.gov
Start Date
February 2009
End Date
November 2012
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Shandong University
Responsible Party
Principal Investigator
Principal Investigator

Ming Hou

Director

Shandong University

Eligibility Criteria

Inclusion Criteria

  • patients who fulfilled entry criteria of acquired aplastic anemia age range 16-70 years

Exclusion Criteria

  • Patients complicated with diabetes, tumor, pregnancy, active infection, or connective tissue diseases, such as systemic lupus erythematosus.

Outcomes

Primary Outcomes

hematologic response

Time Frame: 6 months following antithymocyte globulin plus cyclosporine treatment

hematologic response at 6 months following antithymocyte globulin plus cyclosporine treatment, defined as no longer meeting the criteria for severe aplastic anemia

Study Sites (1)

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