NCT05063591 · 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
- From the date of study enrollment until the date of death.
- Other-event reporting threshold
- 0%
Information about adverse effects associated with blood transfusions were collected, only for participants in Arm A (Intervention Arm). Adverse events in the "Caregiver" arm were not collected.
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Intervention Arm | 0 / 10 | 0 / 10 | 10 / 10 |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- Information about adverse effects associated with blood transfusions were collected, only for participants in Arm A (Intervention Arm). Adverse events in the "Caregiver" arm were not collected.
- event Groups
- deaths Num Affected
- 10
- deaths Num At Risk
- 10
- description
- Patients with aggressive hematologic malignancies who are hospice eligible, not pursuing further cancer directed therapy, and whose primary hematologist is planning to initiate a conversation regarding transition to hospice will be eligible for enrollment. Transfusion support: Patients will be offered symptom-driven transfusion support in addition to standard hospice care
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 10
- serious Num Affected
- 0
- serious Num At Risk
- 10
- title
- Intervention Arm
- frequency Threshold
- 0
- time Frame
- From the date of study enrollment until the date of death.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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