- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02401932
Retrospective Analysis for Patients With Hemophagocytosis in Bone Marrow
November 8, 2015 updated by: Samsung Medical Center
Comparison of Malignant and Non-malignant Disorders Associated Bone Marrow Hemophagocytosis: A Single Center Experience
Comparison of malignant and non-malignant disorders associated bone marrow hemophagocytosis.
Study Overview
Detailed Description
This is a retrospective study comparing malignant and non-malignant disorders associated bone marrow hemophagocytosis.
The medical record of patients who had documented evidences of hemophagocytosis in bone marrow are reviewed.
The clinical and biological characteristics are compared according to the underlying disorders of hemophagocytosis.
Study Type
Observational
Enrollment (Actual)
300
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Seoul, Korea, Republic of, 135-710
- Samsung Medical Center
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
The investigators reviewed the electronic data base of medical records at the Samsung Medical Center, and selected 264 patients who had evidence of hemophagocytic histiocytosis in bone marrow aspiration and biopsy between January 2000 and June 2014.
Description
Inclusion Criteria:
- patients who had evidence of hemophagocytic histiocytosis in bone marrow aspiration and biopsy
Exclusion Criteria:
- patients who did not evidence of hemophagocytic histiocytosis in bone marrow aspiration and biopsy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Hemophagocytosis
The group includes patients who have the evidence of hemophagocytosis in their bone marrow or other sites.
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Best supportive care and immunosuppressive treatments
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Overall survival
Time Frame: 12 Months
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12 Months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2014
Primary Completion (ACTUAL)
September 1, 2015
Study Completion (ACTUAL)
September 1, 2015
Study Registration Dates
First Submitted
March 9, 2015
First Submitted That Met QC Criteria
March 24, 2015
First Posted (ESTIMATE)
March 30, 2015
Study Record Updates
Last Update Posted (ESTIMATE)
November 10, 2015
Last Update Submitted That Met QC Criteria
November 8, 2015
Last Verified
November 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- 2015-02-013
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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