Trial Condition(s):
Study to evaluate endometrial safety of a transdermally administered Estradiol / Levonorgestrel preparation in hormone therapy in postmenopausal women
92001
Not Available
Not Available
Please see attached Study Results Summary below.
No Inclusion Criteria Available
No Exclusion Criteria Available
Locations | Status | ||
---|---|---|---|
Locations Investigative Site Leicester, United Kingdom, LE1 5WW | Status Completed | Contact Us: E-mail: Not Available Phone: Not Available | |
Locations Investigative Site Manchester, United Kingdom, M15 6SX | Status Completed | Contact Us: E-mail: Not Available Phone: Not Available | |
Locations Investigative Site Birmingham, United Kingdom, B15 2SQ | Status Completed | Contact Us: E-mail: Not Available Phone: Not Available | |
Locations Investigative Site Waterloo, United Kingdom, L22 0LG | Status Completed | Contact Us: E-mail: Not Available Phone: Not Available |
An open-label, multi-center study to describe endometrial safety of a transdermally administered estradiol / levonorgestrel preparation in hormone therapy over 24 months (26 cycles) in postmenopausal women
Trial Type:
Interventional
Intervention Type:
N/A
Trial Purpose:
N/A
Allocation:
N/A
Blinding:
N/A
Assignment:
N/A
Trial Arms:
N/A