NCT00509665 · OUTCOME
Progression-free Survival
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEDIAN
- Unit
- months
- Interval / dispersion
- 95% Confidence Interval
- Time frame
- Through the end of follow up, for an average of 8 months
Analysis population: Only patients who had re-staging scans are included in the number of participants analyzed.
Groups in this outcome
Gemcitabine+Doxorubicin
doxorubicin hydrochloride: given as 25mgm2 IV on days 1 and 8 of each 21-day cycle. gemcitabine hydrochloride: given as 100mg/m2 IV over days 1 and 8 of each 21 day cycle
| Group | Source count |
|---|---|
| Gemcitabine+Doxorubicin | 17 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Gemcitabine+Doxorubicin | 1.6 | Not reported | 1.4 | 4.2 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 1.4
- upper Limit
- 4.2
- value
- 1.6
- denoms
- counts
- group Id
- OG000
- value
- 17
- units
- Participants
- dispersion Type
- 95% Confidence Interval
- groups
- description
- doxorubicin hydrochloride: given as 25mgm2 IV on days 1 and 8 of each 21-day cycle. gemcitabine hydrochloride: given as 100mg/m2 IV over days 1 and 8 of each 21 day cycle
- id
- OG000
- title
- Gemcitabine+Doxorubicin
- param Type
- MEDIAN
- population Description
- Only patients who had re-staging scans are included in the number of participants analyzed.
- reporting Status
- POSTED
- time Frame
- Through the end of follow up, for an average of 8 months
- title
- Progression-free Survival
- type
- SECONDARY
- unit Of Measure
- months
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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