NCT00609739 · OUTCOME
Patients With Regimen-Related Toxicity
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
- Up to 30 Days Post Study Treatment
What was measured
Number of patients with adverse events related to treatment.
Groups in this outcome
Cytarabine + Mitoxantrone
Patients receive administration of high dose cytosine arabinoside and mitoxantrone followed by hematopoietic cell transplant.
| Group | Source count |
|---|---|
| Cytarabine + Mitoxantrone | 1 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Cytarabine + Mitoxantrone | 0 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 0
- denoms
- counts
- group Id
- OG000
- value
- 1
- units
- Participants
- description
- Number of patients with adverse events related to treatment.
- groups
- description
- Patients receive administration of high dose cytosine arabinoside and mitoxantrone followed by hematopoietic cell transplant.
- id
- OG000
- title
- Cytarabine + Mitoxantrone
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- Up to 30 Days Post Study Treatment
- title
- Patients With Regimen-Related Toxicity
- type
- SECONDARY
- unit Of Measure
- participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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