Laxity; Skin Clinical Trial
Official title:
Comparison Of Aesthetic Techniques For Rejuvenation Of Genital Region: A Randomized Clinical Trial
NCT number | NCT04998578 |
Other study ID # | Caap |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | October 1, 2021 |
Est. completion date | October 1, 2024 |
The microneedle is a minimally invasive technique, consists of the application of a roller surrounded by small and thin needles that pierce the skin and generate a mechanical stimulus with no ablative effect on the skin. The study aims to test the hypothesis that the technique of microneedle in the treatment of tissue flaccidity and hyperchromia of female external genitalia is safe and with a more effective result in clinical improvement through genital rejuvenation and unification of skin tone when compared to non-ablative radiofrequency technique.
Status | Recruiting |
Enrollment | 112 |
Est. completion date | October 1, 2024 |
Est. primary completion date | October 1, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: • Women aged 18-65 years with skin flaccidity and genital hyperchromia Exclusion Criteria: - Patients who use cosmetics in the genital region - Use of anticoagulant medication - Use of pacemakers - Pregnancy - Dermatoses in the region to be treated and / or local inflammatory condition, without diagnosis of infection - Difficulty in understanding the proposed instruments |
Country | Name | City | State |
---|---|---|---|
Brazil | Centro de Atenção ao Assoalho Pelvico | Salvador | Ba |
Brazil | Centro de Atenção ao assoalho pélvico | Salvador | Bahia |
Lead Sponsor | Collaborator |
---|---|
Centro de Atenção ao Assoalho Pélvico |
Brazil,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | External genital Laxity | It will be evaluated by turgor, number of skinfolds, evidenced by self report, comparison of images taken before and after the procedure and satisfaction of the patient, verified in the Likert scale and Visual Analog Scale. | 1, 3, 6 and 12 months after treatment | |
Primary | Genital Hyperchromia | It will be evaluated the uniformity of the skin tone, evidenced by the self report, comparison of images taken before after the procedure and satisfaction of the participant, verified in the scale of Likert and Scale Visual Analog. | 1, 3, 6 and 12 months after treatment | |
Secondary | Sexual function | It will be evaluated through the questionnaire Sexual Quotient - Female Version (QS-F), Female Sexual Function Index (FSFI) | 1, 3, 6 and 12 months after treatment | |
Secondary | Female Genital Self-Image | It will be evaluated through the Female Genital Self-Image Scale (FGSIS) > 26 | 1, 3, 6 and 12 months after treatment | |
Secondary | Melasma Quality of Life | It will be evaluated through the Melasma Quality of Life Scale (MELASQoL). | 1, 3, 6 and 12 months after treatment |
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