Clinical trial
A Randomised, Double Blinded, Six-armed Placebo Controlled Study to Investigate Optimal Dose of Tamoxifen With the Most Favourable Side Effect Spectre and With Mammography Density Reduction Non-inferior to That of 20 mg Tamoxifen
NCT03346200 is registered in ClinicalTrials.gov with Per Hall as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomised, Double Blinded, Six-armed Placebo Controlled Study to Investigate Optimal Dose of Tamoxifen With the Most Favourable Side Effect Spectre and With Mammography Density Reduction Non-inferior to That of 20 mg Tamoxifen
- Lead sponsor
- Per Hall
- Phase
- Phase 2
- Overall status
- Completed
- Start date
- November 30, 2016
- Completion date
- December 31, 2019
- Enrollment
- 1,440 (actual)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
mammographic density reduction, risk reduction