NCT00423930 · OUTCOME
Overall Survival Rate: Percentage of Participants Who Survived
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
- 95% Confidence Interval
- Time frame
- 2 years
Groups in this outcome
IMRT + Cisplatin + Bevacizumab
This is a single-institution phase II study. The primary endpoint is to determine 2-year progression-free survival for patients with locally or regionally advanced HNSCC treated with concurrent intensity modulated radiation therapy (IMRT) + cisplatin + bevacizumab. bevacizumab cisplatin conventional surgery intensity-modulated radiation therapy
| Group | Source count |
|---|---|
| IMRT + Cisplatin + Bevacizumab | 42 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| IMRT + Cisplatin + Bevacizumab | 88 | Not reported | 78.6 | 98.4 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 78.6
- upper Limit
- 98.4
- value
- 88
- denoms
- counts
- group Id
- OG000
- value
- 42
- units
- Participants
- dispersion Type
- 95% Confidence Interval
- groups
- description
- This is a single-institution phase II study. The primary endpoint is to determine 2-year progression-free survival for patients with locally or regionally advanced HNSCC treated with concurrent intensity modulated radiation therapy (IMRT) + cisplatin + bevacizumab. bevacizumab cisplatin conventional surgery intensity-modulated radiation therapy
- id
- OG000
- title
- IMRT + Cisplatin + Bevacizumab
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- 2 years
- title
- Overall Survival Rate: Percentage of Participants Who Survived
- 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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