A double-blind, placebo-controlled study with A-2 on symptoms of vaginal atrophy in postmenopausal wome
Not Applicable
- Conditions
- Healthy postmenopausal women
- Registration Number
- JPRN-UMIN000031295
- Lead Sponsor
- Department of Obstetrics and Gynecology, Tokyo Dental College Ichikawa General Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
1) Diversity from normal ranges of vital signs, and in clinical laboratory tests 2) Current or past reproductive-related cancer and so forth 3) Serious illumes 4) Allergies to soy or lactose 5) Individuals who are diagnosed as inappropriate for the trial by the principal Investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method