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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01995331 |
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Date of registration:
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21/11/2013 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Moderate-dose Cyclophosphamide for Childhood Acquired Aplastic Anemia
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Scientific title:
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Moderate-dose Cyclophosphamide for Childhood Acquired Aplastic Anemia |
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Date of first enrolment:
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March 2012 |
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Target sample size:
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30 |
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Recruitment status: |
Active, not recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01995331 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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Phase 4
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Countries of recruitment
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China
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Contacts
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Name:
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Xiaifan Zhu, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Department of Pediatrics, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Acquired Childhood Severe Aplastic Anemia (SAA)
Exclusion Criteria:
- not Childhood and Acquired Severe Aplastic Anemia
Age minimum:
1 Year
Age maximum:
18 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Aplastic Anemia
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Intervention(s)
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Drug: cyclophosphamide,cyclosporine A
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Primary Outcome(s)
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The reponse of Moderate-dose Cyclophosphamide for Childhood Acquired Aplastic Anemia
[Time Frame: 36 months]
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Secondary Outcome(s)
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The side effect of Moderate-dose Cyclophosphamide for Childhood Acquired Aplastic Anemia
[Time Frame: 36 months]
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Secondary ID(s)
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YL20102601
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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