NCT02349412 · 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
- Adverse events were not collected for this study.
- Other-event reporting threshold
- 0%
Adverse events were not collected for this study.
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Arm 1 (Early Palliative Care) | 0 / 0 | 0 / 0 | 0 / 0 |
| Arm 2 (Usual Care) | 0 / 0 | 0 / 0 | 0 / 0 |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- Adverse events were not collected for this study.
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 0
- description
- Patients receive early palliative care and standard oncology care. Patients and family caregivers will be asked to complete quality-of-life questionnaires at weeks 6, 12, and 24. Survival follow-up will be every 4 months from week 24 until death or up to 3 years.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 0
- serious Num Affected
- 0
- serious Num At Risk
- 0
- title
- Arm 1 (Early Palliative Care)
- deaths Num Affected
- 0
- deaths Num At Risk
- 0
- description
- Patients receive standard oncology care. Patient and family caregiver will be asked to complete self-report questionnaires at weeks 6, 12, and 24. Survival follow-up will be every 4 months from week 24 until death or up to 3 years. Palliative care visit only upon request from attending oncologist(s) or patient/family.
- id
- EG001
- other Num Affected
- 0
- other Num At Risk
- 0
- serious Num Affected
- 0
- serious Num At Risk
- 0
- title
- Arm 2 (Usual Care)
- frequency Threshold
- 0
- time Frame
- Adverse events were not collected for this study.
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Preserved source evidence · Not medical advice
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