Efficacy and Safety of Desferal Versus Osveral in Transfusional Iron Overload
NCT01369719 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 138
Last updated 2011-06-14
Summary
Thalassemic patients often suffer from iron overload due to frequent blood transfusion. Oral iron chelators reduce iron overload in transfusion dependent patients. The aim of this study is to compare the efficacy and safety of osveral and desferal in transfusional iron overload patients with β-Thalassemia and intermediate Thalassemia in Bandarabbas.
Conditions
- Thalassemia
- Iron Overload
- Transfusion Related Complications
Interventions
- DRUG
-
osveral
receive 20 mg/kg daily orally
- DRUG
-
Desferal
40-50mg/Kg for 6 nights in each week subcutaneously
Sponsors & Collaborators
-
Hormozgan University of Medical Sciences
lead OTHER
Principal Investigators
-
Fariba Mansoori, Resident · Hormozgan University of Medical Sciences (HUMS)
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 2 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-02-28
- Primary Completion
- 2011-01-31
- Completion
- 2011-05-31
Countries
- Iran
Study Locations
More Related Trials
-
Comparison of Deferasirox and Desferoxamine in Patients of β-Thalassemia Major With Iron Overload
NCT06468423 ·Status: COMPLETED ·Phase: NA
-
Combined Chelation Therapy in Patients With Transfusion Dependent Thalassemia and Iron Overload
NCT00901199 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Deferasirox in Non-transfusion Dependent Thalassemia Patients With Iron Overload and a One Year Open-label Extension Study
NCT00873041 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Pharmacodynamic Study of an Oral Iron Chelator Given for 6 Months to Patients With Iron Overload
NCT01186419 ·Status: COMPLETED ·Phase: PHASE2
-
Combination Deferasirox and Deferiprone for Severe Iron Overload in Thalassemia
NCT01709032 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
An Extension Study of Iron Chelation Therapy With Deferasirox (ICL670) in β-thalassemia Patients With Transfusional Iron Overload
NCT00171210 ·Status: COMPLETED ·Phase: PHASE3
-
A Study of Long-term Treatment With Deferasirox in Patients With Beta-thalassemia and Transfusional Hemosiderosis
NCT00171171 ·Status: COMPLETED ·Phase: PHASE3
-
This Study Will Evaluate Efficacy and Safety of Deferasirox in Patients With Myelodysplastic Syndromes (MDS), Thalassemia and Rare Anemia Types Having Transfusion-induced Iron Overload.
NCT01250951 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Pharmacokinetic Study of Escalating Multiple Doses of an Iron Chelator in Patients With Iron Overload
NCT01039636 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacotherapy Prescribing Pattern and the Adherence Level to Iron Chelation Therapy in Thalassemia
NCT06210139 ·Status: COMPLETED
-
Combination Iron Chelation Therapy
NCT00004982 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluation of Subcutaneous Desferrioxamine as Treatment for Transfusional Hemochromatosis
NCT00000595 ·Status: COMPLETED ·Phase: PHASE2
-
A Study Assessing the Efficacy and Safety of Deferasirox in Patients With Transfusion-dependent Iron Overload
NCT00171821 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety Study of Deferasirox in Patients With Non-transfusion Dependent Thalassemia
NCT01709838 ·Status: COMPLETED ·Phase: PHASE4
-
Phase I Study to Examine the Effect of Deferasirox on Renal Hemodynamics in β-thalassemia Patients With Transfusional Iron Overload
NCT00560820 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluating Use of Deferasirox as Compared to Deferoxamine in Treating Cardiac Iron Overload
NCT00600938 ·Status: COMPLETED ·Phase: PHASE2
-
Extension Study of the Efficacy and Safety of Deferasirox Treatment in Beta-thalassemia Patients With Transfusional Hemosiderosis (Study Amended to 2-year Duration)
NCT00171301 ·Status: COMPLETED ·Phase: PHASE4
-
Long-term Clinical Study of CN128 in Thalassemia Patients
NCT04614779 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Oral Deferasirox (20 mg/kg/d) in Pts 3 to 6 Months After Allogeneic Hematopoietic Cell Transplantation Who Present With Iron Overload
NCT00654589 ·Status: COMPLETED ·Phase: PHASE4
-
Post Hematopoietic Stem Cell Transplantation
NCT01610297 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Efficacy of Deferasirox in Combination With Desferoxamine in β-thalassaemia Patients With Severe Cardiac Iron Overload
NCT01459718 ·Status: TERMINATED ·Phase: PHASE2
-
Iron Balance Study of DFO and GT56-252 in Patients With Transfusional Iron Overload Secondary to Beta-Thalassemia
NCT00069862 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Intensive Combined Chelation Therapy for Iron-Induced Cardiac Disease in Patients With Thalassemia Major
NCT00800761 ·Status: COMPLETED ·Phase: PHASE4
-
Clinical Trial of Deferasirox Combination Treatment With Deferiprone In Thalassaemia Patients
NCT02198508 ·Status: COMPLETED ·Phase: NA
-
Long-term Clinical Study of CN128 in Thalassemia With Sever Liver Iron Overloaded Patients
NCT05355766 ·Status: COMPLETED ·Phase: PHASE2