Trial Condition(s):
Postmenopause, Hormone Replacement Therapy, Sexuality
Study to assess the influence of an Estroprogestogenic biphasic solution on clinical laboratory and sexual parameters in postmenopausal women
Bayer Identifier:
90659
ClinicalTrials.gov Identifier:
Not Available
EudraCT Number:
Not Available
EU CT Number:
Not Available
Study Completed
Trial Purpose
Please see attached Study Results Summary below.
Inclusion Criteria
No Inclusion Criteria Available
Exclusion Criteria
No Exclusion Criteria Available
Trial Summary
Enrollment Goal
40
Trial Dates
Phase
4
Could I receive a placebo?
No
Products
Climen (EV/CA, BAY86-4978)
Accepts Healthy Volunteers
N/A
Where to Participate
Locations
| Locations |
|---|
Trial Design
Clinical and laboratorial evaluation of an estroprogestogenic biphasic solution for patients in postmenopause, with emphasis in sexuality. A single-center, crossover, placebo-controlled study
Trial Type:
Interventional
Intervention Type:
N/A
Trial Purpose:
N/A
Allocation:
N/A
Blinding:
N/A
Assignment:
N/A
Trial Arms:
N/A
Primary Outcome
- Timeframe:
Secondary Outcome
- Timeframe:
Additional Information
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