RBR-2wjrp4
Not yet recruiting
未知
Randomized controlled clinical trial, with topical use of estrogen,testosterone, polyacryli cacid and placebo in the treatment of urogenital atrophy in postmenopausal women
Hospital da Mulher Prof. Dr. José Aristodemo Pinotti - CAISM Unicamp0 sitesJanuary 4, 2012
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- In postmenopausal women with symptoms of urogenital atrophy
- Sponsor
- Hospital da Mulher Prof. Dr. José Aristodemo Pinotti - CAISM Unicamp
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Physiological menopause with amenorrhea over three years
- •FSH\> 30 IU
- •Aged over 40 years and less than 75 years.
- •Women are not on medication for hormonal treatment of menopausal symptoms in the last 6 months
- •Women who have mammography and Pap smear in the last 12 months with appropriate result
- •Women with symptoms of urogenital atrophy.
Exclusion Criteria
- •The patient's explicit refusal to participate
- •Patient with bilateral oophorectomy
- •Patients with a BMI less than 18\.5 kg / m² or greater than 30 kg / m²
- •Women who present contraindication to the use of topical estrogen, as follows: Absolute (recent myocardial infarction, severe hypertension, diabetes mellitus is difficult to control, history of thromboembolic disease, recent Liver failure, or severe, or activity, prior breast cancer , Cancer of the endometrium prior mammary dysplasia with atypical hyperplasia, genital bleeding of unknown origin) or relative (family history of breast cancer, endometrial hyperplasia prior Cholelithiasis)
- •Women who have ulcerative colitis, Crohn's disease or diarrhea due to intestinal disease
- •Women who have positive serology for HIV, Hepatitis B and C
- •Patients on medication for depression or other psychiatric disorders
Outcomes
Primary Outcomes
Not specified
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