NCT00670631 · BASELINE
Baseline characteristics
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- denoms
- counts
- group Id
- BG000
- value
- 0
- units
- Participants
- groups
- description
- Induction: DPACE(dexamethasone,cisplatin,doxorubicin,cyclophosphamide,etoposide) chemotherapy plus stem cell collection. Additional stem cell collection and/or chemotherapy may be required. After collection, participants will receive dexamethasone x 4 days every 14 days.
- id
- BG000
- title
- Tandem Autologous Stem Cell Transplant
- measures
- classes
- categories
- title
- <=18 years
- title
- Between 18 and 65 years
- title
- >=65 years
- title
- Age, Categorical
- title
- Age, Continuous
- classes
- categories
- title
- Female
- title
- Male
- title
- Sex: Female, Male
- classes
- title
- United States
- title
- Region of Enrollment
- unit Of Measure
- participants
- population Description
- Data not available. Study conducted at University of Utah. Upon PI leaving Utah and coming to the University of Iowa, record NCT00670631 was transferred to Iowa by ClinicalTrials.gov staff. No research activities under NCT00670631 were conducted at Iowa. PRS staff at Iowa and Utah have corresponded and neither party (including PI) have the data.
Complete source fields
- denoms
- counts
- group Id
- BG000
- value
- 0
- units
- Participants
- groups
- description
- Induction: DPACE(dexamethasone,cisplatin,doxorubicin,cyclophosphamide,etoposide) chemotherapy plus stem cell collection. Additional stem cell collection and/or chemotherapy may be required. After collection, participants will receive dexamethasone x 4 days every 14 days.
- id
- BG000
- title
- Tandem Autologous Stem Cell Transplant
- measures
- classes
- categories
- title
- <=18 years
- title
- Between 18 and 65 years
- title
- >=65 years
- title
- Age, Categorical
- title
- Age, Continuous
- classes
- categories
- title
- Female
- title
- Male
- title
- Sex: Female, Male
- classes
- title
- United States
- title
- Region of Enrollment
- unit Of Measure
- participants
- population Description
- Data not available. Study conducted at University of Utah. Upon PI leaving Utah and coming to the University of Iowa, record NCT00670631 was transferred to Iowa by ClinicalTrials.gov staff. No research activities under NCT00670631 were conducted at Iowa. PRS staff at Iowa and Utah have corresponded and neither party (including PI) have the data.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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