NCT02624388 · OUTCOME
Percentage of Participants Requiring Reduced Treatment Doses Due to an Adverse Event
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- percentage of participants
- Interval / dispersion
- Not reported
- Time frame
- From the first date study drug is taken until the last date that study drug is taken, about 8 - 12 weeks if there are no chemotherapy delays
Groups in this outcome
Arm A: Genistein Followed by Placebo - GENISTEIN Cycles
Genistein daily throughout chemotherapy cycles 1 and 2, and placebo daily during chemotherapy cycles 3 and 4 Genistein: Estrogen-like compound (isoflavone) derived from soybeans Placebo: Pill that contains no medicine
Arm B: Placebo Followed by Genistein - GENISTEIN Cycles
Placebo daily throughout chemotherapy cycles 1 and 2, and genistein daily during chemotherapy cycles 3 and 4 Genistein: Estrogen-like compound (isoflavone) derived from soybeans Placebo: Pill that contains no medicine
Arm A: Genistein Followed by Placebo - PLACEBO Cycles
Genistein daily throughout chemotherapy cycles 1 and 2, and placebo daily during chemotherapy cycles 3 and 4 Genistein: Estrogen-like compound (isoflavone) derived from soybeans Placebo: Pill that contains no medicine
Arm B: Placebo Followed by Genistein - PLACEBO Cycles
Genistein daily throughout chemotherapy cycles 1 and 2, and placebo daily during chemotherapy cycles 3 and 4 Genistein: Estrogen-like compound (isoflavone) derived from soybeans Placebo: Pill that contains no medicine
| Group | Source count |
|---|---|
| Arm A: Genistein Followed by Placebo - GENISTEIN Cycles | 2 |
| Arm B: Placebo Followed by Genistein - GENISTEIN Cycles | 2 |
| Arm A: Genistein Followed by Placebo - PLACEBO Cycles | 2 |
| Arm B: Placebo Followed by Genistein - PLACEBO Cycles | 2 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Arm A: Genistein Followed by Placebo - GENISTEIN Cycles | 0 | Not reported | Not reported | Not reported | Not reported |
| Arm B: Placebo Followed by Genistein - GENISTEIN Cycles | 0 | Not reported | Not reported | Not reported | Not reported |
| Arm A: Genistein Followed by Placebo - PLACEBO Cycles | 0 | Not reported | Not reported | Not reported | Not reported |
| Arm B: Placebo Followed by Genistein - PLACEBO Cycles | 0 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 0
- group Id
- OG001
- value
- 0
- group Id
- OG002
- value
- 0
- group Id
- OG003
- value
- 0
- denoms
- counts
- group Id
- OG000
- value
- 2
- group Id
- OG001
- value
- 2
- group Id
- OG002
- value
- 2
- group Id
- OG003
- value
- 2
- units
- Participants
- groups
- description
- Genistein daily throughout chemotherapy cycles 1 and 2, and placebo daily during chemotherapy cycles 3 and 4 Genistein: Estrogen-like compound (isoflavone) derived from soybeans Placebo: Pill that contains no medicine
- id
- OG000
- title
- Arm A: Genistein Followed by Placebo - GENISTEIN Cycles
- description
- Placebo daily throughout chemotherapy cycles 1 and 2, and genistein daily during chemotherapy cycles 3 and 4 Genistein: Estrogen-like compound (isoflavone) derived from soybeans Placebo: Pill that contains no medicine
- id
- OG001
- title
- Arm B: Placebo Followed by Genistein - GENISTEIN Cycles
- description
- Genistein daily throughout chemotherapy cycles 1 and 2, and placebo daily during chemotherapy cycles 3 and 4 Genistein: Estrogen-like compound (isoflavone) derived from soybeans Placebo: Pill that contains no medicine
- id
- OG002
- title
- Arm A: Genistein Followed by Placebo - PLACEBO Cycles
- description
- Genistein daily throughout chemotherapy cycles 1 and 2, and placebo daily during chemotherapy cycles 3 and 4 Genistein: Estrogen-like compound (isoflavone) derived from soybeans Placebo: Pill that contains no medicine
- id
- OG003
- title
- Arm B: Placebo Followed by Genistein - PLACEBO Cycles
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- From the first date study drug is taken until the last date that study drug is taken, about 8 - 12 weeks if there are no chemotherapy delays
- title
- Percentage of Participants Requiring Reduced Treatment Doses Due to an Adverse Event
- type
- SECONDARY
- unit Of Measure
- percentage of participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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