NCT00984399 · 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
- 2 years
- Other-event reporting threshold
- 0%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Letrozole | 0 / 12 | 0 / 12 | 0 / 12 |
| Anastrozole | 0 / 19 | 0 / 19 | 0 / 19 |
Serious adverse events
Other reported adverse events
Complete source fields
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 12
- description
- This is a prospective longitudinal pilot study, and the targeted patient population is postmenopausal women with breast cancer being treated with adjuvant aromatase inhibitors who are initiated on vaginal 17β-estradiol to relieve symptoms of atrophic vaginitis.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 12
- serious Num Affected
- 0
- serious Num At Risk
- 12
- title
- Letrozole
- deaths Num Affected
- 0
- deaths Num At Risk
- 19
- description
- This is a prospective longitudinal pilot study, and the targeted patient population is postmenopausal women with breast cancer being treated with adjuvant aromatase inhibitors who are initiated on vaginal 17β-estradiol to relieve symptoms of atrophic vaginitis.
- id
- EG001
- other Num Affected
- 0
- other Num At Risk
- 19
- serious Num Affected
- 0
- serious Num At Risk
- 19
- title
- Anastrozole
- frequency Threshold
- 0
- time Frame
- 2 years
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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