NCT01869777 · ADVERSE EVENTS
Adverse events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.
- Collection time frame
- Up to 2 years to assess for survival only
- Other-event reporting threshold
- 0%
Adverse events were not monitored/assessed for this trial.
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Diagnostic (Bioelectric Impedance Analysis) | 0 / 0 | 0 / 0 | 16 / 101 |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- Adverse events were not monitored/assessed for this trial.
- event Groups
- deaths Num Affected
- 16
- deaths Num At Risk
- 101
- description
- Patients undergo bioelectrical impedance phase angle measurement on day 1 of treatment. Patients with AML undergo a second measurement just prior to the nadir marrow. Patients also undergo bioelectrical impedance measurements prior to any invasive procedures (bone marrow biopsy, leukapheresis, PICC line placement, etc.). bioelectric impedance analysis: Undergo bioelectric impedance analysis
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 0
- serious Num Affected
- 0
- serious Num At Risk
- 0
- title
- Diagnostic (Bioelectric Impedance Analysis)
- frequency Threshold
- 0
- time Frame
- Up to 2 years to assess for survival only
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle