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Postmenopausal women with vascular symptoms will use Cimifuga Racemosa or Placebo and the effects will be evaluated using Flow-Mediated Dilatation of the brachial artery.
The interruption of the secretion of ovarian steroids after menopause, determines a change in the vascular pattern in several levels. Thus, several vascular effects might interfere with women's health. The use of hormone replacement therapy has contributed to the improvement in these effects. In previous studies, the investigators observed the effects of hormonal replacement therapy in improving such effects in postmenopausal women. The aim of the present study is to evaluate the effects of CIMICIFUGA RACEMOSA on the Flow-Mediated Dilatation of the brachial artery.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental | Experimental | Women will use Cimifuga Racemosa for 28 days and will be submitted to measurement of the diameter of the brachial artery before and after treatment |
|
| Placebo | Placebo Comparator | Women will use Placebo for 28 days and will be submitted to measurement of the diameter of the brachial artery before and after treatment |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cimifuga Racemosa | Drug | Experimental group will use 160mg of Cimifuga Racemosa for 28 days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Measurement of the brachial artery using flow-mediated dilation of post menopausal women, before and after use of Cimifuga Racemosa | We will evaluate the vascular effect of Cimifuga Racemosa on the brachial artery. The diameter of the artery will be measured before and one month after use of Cimifuga Racemosa and, in both situations, before and after the use of a cuff in the forearm. Measurement will be in millimeters. | 28 days |
| Measure | Description | Time Frame |
|---|---|---|
| Frequency of symptoms and side effects | Patients symptoms before and after the use of Cimifuga Racemosa | 28 days |
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Inclusion Criteria:
Exclusion Criteria:
only postmenopausal women will be included
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| Name | Affiliation | Role |
|---|---|---|
| Selmo Geber, MD PhD | Universidde Federal de Minas Gerais | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital das Clinicas - Universidade Federal de Minas Gerais | Belo Horizonte | Minas Gerais | 30130100 | Brazil |
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| Placebo | Drug | patients of the placebo group will use placebo once a day for 28 days |
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