NCT01553539 · OUTCOME
Number of Participants Who Experienced Adverse Events as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Participants experiencing adverse events
- Interval / dispersion
- Not reported
- Time frame
- Approximately 1 year
What was measured
See the adverse event tables for specifics.
Groups in this outcome
Treatment (Antiangiogenesis Therapy)
Patients receive therapeutic angiotensin-(1-7) SC once daily in the absence of disease progression or unacceptable toxicity.
| Group | Source count |
|---|---|
| Treatment (Antiangiogenesis Therapy) | 20 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Treatment (Antiangiogenesis Therapy) | 20 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 20
- denoms
- counts
- group Id
- OG000
- value
- 20
- units
- Participants
- description
- See the adverse event tables for specifics.
- groups
- description
- Patients receive therapeutic angiotensin-(1-7) SC once daily in the absence of disease progression or unacceptable toxicity.
- id
- OG000
- title
- Treatment (Antiangiogenesis Therapy)
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- Approximately 1 year
- title
- Number of Participants Who Experienced Adverse Events as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0
- type
- PRIMARY
- unit Of Measure
- Participants experiencing adverse events
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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