Iron Overload Clinical Trial
Official title:
Changes in Pituitary Iron and Volume With Deferasirox in Transfusional Iron Overload
NCT number | NCT01376622 |
Other study ID # | CCI-08-00143 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | November 2008 |
Est. completion date | July 1, 2011 |
Verified date | October 2023 |
Source | Children's Hospital Los Angeles |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Despite continuing advances in iron chelation therapy, iron toxicity of endocrine glands, particularly the pituitary gland, remains common in patients with transfusion dependent anemias. We would like to establish accurate population norms of pituitary R2 and volume and understand the progression of pituitary iron in transfused patients on Deferasirox.
Status | Completed |
Enrollment | 130 |
Est. completion date | July 1, 2011 |
Est. primary completion date | July 1, 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 2 Years to 25 Years |
Eligibility | Inclusion Criteria: - Currently on chronic transfusion therapy. - Duration of chronic transfusion >1 year. - Age 2 to 25 years - On deferasirox monotherapy for the duration of the study. - Informed consent from legal guardian and/or patient. - On deferasirox for a minimum of 3 months at start of study. Exclusion Criteria: - Sickle cell disease or sickle-beta zero genotype. - Combination of deferasirox and another iron chelator. |
Country | Name | City | State |
---|---|---|---|
United States | Children's Hospital Los Angeles | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
Children's Hospital Los Angeles | Novartis Pharmaceuticals |
United States,
Wood JC, Noetzl L, Hyderi A, Joukar M, Coates T, Mittelman S. Predicting pituitary iron and endocrine dysfunction. Ann N Y Acad Sci. 2010 Aug;1202:123-8. doi: 10.1111/j.1749-6632.2010.05545.x. — View Citation
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