NCT00113841 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Curcumin starting dose 2 grams orally in two divided doses (a.m., p.m.)
- id
- FG000
- title
- Curcumin
- description
- Curcumin starting dose 2 grams orally in 2 divided doses (a.m., p.m.) and Bioperine 5 mg orally twice daily
- id
- FG001
- title
- Curcumin + Bioperine
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 2
- type
- Disease progression
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Non-compliant
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 16
- group Id
- FG001
- num Subjects
- 17
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 15
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Of 42 patients enrolled, 9 were excluded from the trial prior to group assignment because of screen failure.
- recruitment Details
- Recruitment period: 11/2004 to 1/2008. All participants were recruited at UT MD Anderson Cancer Center.
Complete source fields
- groups
- description
- Curcumin starting dose 2 grams orally in two divided doses (a.m., p.m.)
- id
- FG000
- title
- Curcumin
- description
- Curcumin starting dose 2 grams orally in 2 divided doses (a.m., p.m.) and Bioperine 5 mg orally twice daily
- id
- FG001
- title
- Curcumin + Bioperine
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 2
- type
- Disease progression
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Non-compliant
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 16
- group Id
- FG001
- num Subjects
- 17
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 15
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Of 42 patients enrolled, 9 were excluded from the trial prior to group assignment because of screen failure.
- recruitment Details
- Recruitment period: 11/2004 to 1/2008. All participants were recruited at UT MD Anderson Cancer Center.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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