Safety and Efficacy of Levamisole Combined With Cyclosporine A in Patients With Subclinical Paroxysmal Nocturnal Hemoglobinuria and PNH in the Setting of Another Bone Marrow Failure Syndromes(PNH-2013)
- Conditions
- Paroxysmal Nocturnal HemoglobinuriaHemoglobinuriaHemoglobinuria, ParoxysmalProteinuriaUrination DisordersThrombosisBone Marrow FailureAplastic Anemia,Anemia, Hemolytic
- Interventions
- Drug: Levamisole+cyclosporin A+GlucocorticoidsDrug: Glucocorticoids
- Registration Number
- NCT01760096
- Brief Summary
Paroxysmal nocturnal hemoglobinuria is an acquired chronic hemolytic anemia,this study is designed to evaluate the safety and efficacy of Levamisole combined with cyclosporine A in patients with Subclinical Paroxysmal Nocturnal Hemoglobinuria and PNH in the setting of another bone marrow failure syndromes
- Detailed Description
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disorder of the hematopoietic stem cell characterized by intravascular hemolysis, hemoglobinuria, anemia, and thrombosis, Patients may be at high risk of thrombosis and may develop bone marrow failure or aplastic anemia, with low white blood cell and platelet counts,because the manifestation and pathologic processes are complicate,the treatment is very difficult,this study is designed to evaluate the safety and efficacy of Levamisole combined with cyclosporine A in patients with Subclinical Paroxysmal Nocturnal Hemoglobinuria and PNH in the setting of another bone marrow failure syndromes
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 50
- Clinical and biochemical signs of Subclinical Paroxysmal Nocturnal Hemoglobinuria and PNH in the setting of another bone marrow failure syndromes
- Diagnosis confirmed by Ham's test or Flow cytometry Patients have any Flow cytometry data
- patient should complete levamisole study for at least half a year
- Active infection which requires antibiotic treatment
- Pregnant or lactating women
- Epilepsy and mental illness
- Kidney and liver function abnormal
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Levamisole+cyclosporin A+Glucocorticoids Levamisole+cyclosporin A+Glucocorticoids Levamisole+cyclosporin A+Glucocorticoids cyclosporin A+Glucocorticoids cyclosporin A+Glucocorticoids cyclosporin A+Glucocorticoids Glucocorticoids Glucocorticoids Glucocorticoids
- Primary Outcome Measures
Name Time Method Number of patients in each group in complete or partial remission 6 months she got blood transfusion-independent,the hemoglobin became higher
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Institute of Hematology & Blood Diseases Hospital,
🇨🇳Tianjin, Tianjin, China