Vaginal Dryness Clinical Trial
Official title:
Evaluation of Perceived Effectiveness to Evaluate Viscosity of a Vaginal Moisturizer in Menopaused Women
Verified date | December 2018 |
Source | Farmoquimica S.A. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To evaluate the perception of viscosity of a vaginal moisturizer in postmenopausal women
Status | Not yet recruiting |
Enrollment | 33 |
Est. completion date | January 25, 2019 |
Est. primary completion date | January 25, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 45 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Menopausal participants for at least 6 months; - Participants with complaints of vaginal dryness; - Skin integrity in the region of product analysis; - Agreement to comply the procedures of the trial and attend the clinic on the days and times determined for applications and / or evaluations; - Understanding, agreement and signing of the Informed Consent Term. Exclusion Criteria: - Use of anti-inflammatory / immunosuppressive / antihistamine drugs up to 3 weeks prior to selection; - Pathologies and / or active skin lesions (local and / or disseminated) in the evaluation area; - Immunosuppression by drugs or active diseases; - Decompensated endocrinopathies; - Relevant clinical history or current evidence of alcohol or other drug abuse; - known history or suspected intolerance to products of the same category; - Intense sun exposure up to 15 days before evaluation; - Gynecological treatment up to 4 weeks before evaluation; - Other conditions considered by the researcher to be reasonable for disqualification of study participation. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Farmoquimica S.A. |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To evaluate subjectively the perceived viscosity change | Perceived viscosity change of the research product from the point of view of the target public under normal conditions of use through a questionnaire | Immediately after application, 15 and 30 minutes after application |
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