NCT05274763 · 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 3 months
- Other-event reporting threshold
- 0%
No adverse event was reported.
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Supportive Care (CCSH) | 0 / 30 | 0 / 30 | 0 / 30 |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- No adverse event was reported.
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 30
- description
- Patients undergo 4 to 8 sessions (2-4 per week) of CCSH over 30 minutes with a chaplain while impatient. Quality-of-Life Assessment: Ancillary studies Questionnaire Administration: Ancillary studies Spiritual Therapy: Deliver or undergo CCSH session
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 30
- serious Num Affected
- 0
- serious Num At Risk
- 30
- title
- Supportive Care (CCSH)
- frequency Threshold
- 0
- time Frame
- Up to 3 months
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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