NCT01539317 · 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
- 1 hour
- Other-event reporting threshold
- 0%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Topical Liquid Lidocaine | 0 / 25 | 0 / 25 | Not reported / Not reported |
| Topical Saline | 0 / 25 | 0 / 25 | Not reported / Not reported |
Serious adverse events
Other reported adverse events
Complete source fields
- event Groups
- description
- Topical liquid lidocaine: Comparison of topical liquid lidocaine to placebo on application to the vulvar vestibule
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 25
- serious Num Affected
- 0
- serious Num At Risk
- 25
- title
- Topical Liquid Lidocaine
- description
- Topical liquid lidocaine: Comparison of topical liquid lidocaine to placebo on application to the vulvar vestibule
- id
- EG001
- other Num Affected
- 0
- other Num At Risk
- 25
- serious Num Affected
- 0
- serious Num At Risk
- 25
- title
- Topical Saline
- frequency Threshold
- 0
- time Frame
- 1 hour
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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