NCT00301028 · OUTCOME
Number of Participants With Complete Response
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- participants
- Interval / dispersion
- Not reported
- Time frame
- Study period of 3 Years
What was measured
Number of participants with a complete response. Complete Response (CR): Disappearance of clinical and radiological evidence of tumor.
Groups in this outcome
Cetuximab + Carboplatin/Paclitaxel
Cetuximab beginning weekly dose 400 mg/m\^2 intravenous (IV), and 250 mg/m\^2 weeks 2-6; Weekly Carboplatin AUC 2 and Paclitaxel 135 mg/m\^2 for 6 courses.
| Group | Source count |
|---|---|
| Cetuximab + Carboplatin/Paclitaxel | 47 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Cetuximab + Carboplatin/Paclitaxel | 39 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 39
- denoms
- counts
- group Id
- OG000
- value
- 47
- units
- Participants
- description
- Number of participants with a complete response. Complete Response (CR): Disappearance of clinical and radiological evidence of tumor.
- groups
- description
- Cetuximab beginning weekly dose 400 mg/m\^2 intravenous (IV), and 250 mg/m\^2 weeks 2-6; Weekly Carboplatin AUC 2 and Paclitaxel 135 mg/m\^2 for 6 courses.
- id
- OG000
- title
- Cetuximab + Carboplatin/Paclitaxel
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- Study period of 3 Years
- title
- Number of Participants With Complete Response
- type
- PRIMARY
- unit Of Measure
- participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle