NCT02353572 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients received melphalan IV continuously on days -5 to -2 and bortezomib IV over 3-5 seconds on days -4 and -1. Patients also received dexamethasone IV on day -1 prior to the second dose of bortezomib. Beginning two days after completion of melphalan infusion, patients underwent autologous hematopoietic stem cell transplant.
- id
- FG000
- title
- Melphalan, Bortezomib, Autologous Transplant
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Study terminated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 3
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 3
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Within 35 days of planned therapy, patients were evaluated for eligibility by standard tests: paraprotein assessment, bone marrow biopsy and aspiration, MRI scan, PET/CT scan, echocardiography and pulmonary function test. Patients who were not be able to pursue the tandem autotransplant were eligible for one autotransplant.
- recruitment Details
- Between November 2009 and September 2011, 3 patients were enrolled in the study from University of Colorado Cancer Center
Complete source fields
- groups
- description
- Patients received melphalan IV continuously on days -5 to -2 and bortezomib IV over 3-5 seconds on days -4 and -1. Patients also received dexamethasone IV on day -1 prior to the second dose of bortezomib. Beginning two days after completion of melphalan infusion, patients underwent autologous hematopoietic stem cell transplant.
- id
- FG000
- title
- Melphalan, Bortezomib, Autologous Transplant
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Study terminated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 3
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 3
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Within 35 days of planned therapy, patients were evaluated for eligibility by standard tests: paraprotein assessment, bone marrow biopsy and aspiration, MRI scan, PET/CT scan, echocardiography and pulmonary function test. Patients who were not be able to pursue the tandem autotransplant were eligible for one autotransplant.
- recruitment Details
- Between November 2009 and September 2011, 3 patients were enrolled in the study from University of Colorado Cancer Center
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