NCT00891618 · 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 Event reporting from baseline to last treatment, Week 13 of study. Total active study period was June 4, 2009 to May 09, 2011.
- Other-event reporting threshold
- 5%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Acupuncture | 0 / 21 | 0 / 21 | Not reported / Not reported |
Serious adverse events
Other reported adverse events
Complete source fields
- event Groups
- description
- Three (3) acupuncture sessions per week for 4 weeks (Weeks 1-4), 1 week off (Week 5), then 2 per week for 4 more weeks (Weeks 6-10), total of 20 sessions. Each session lasts 20-30 minutes.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 21
- serious Num Affected
- 0
- serious Num At Risk
- 21
- title
- Acupuncture
- frequency Threshold
- 5
- time Frame
- Adverse Event reporting from baseline to last treatment, Week 13 of study. Total active study period was June 4, 2009 to May 09, 2011.
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Preserved source evidence · Not medical advice
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