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Light Emitting Diode in the Treatment of Vulvodynia

Not Applicable
Not yet recruiting
Conditions
Vulvodynia
Registration Number
NCT06337448
Lead Sponsor
Centro de Atenção ao Assoalho Pélvico
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not yet recruiting
Sex
Female
Target Recruitment
10
Inclusion Criteria

Inclusion Criteria:<br><br> - vulvodynia diagnosis<br><br>Exclusion Criteria:<br><br> - patients diagnosed with vaginal infection<br><br> - difficulty in understanding the proposed instruments<br><br> - patients with chronic degenerative neurological diseases<br><br> - pregnant women

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Number of participants with treatment-related adverse events as assessed by Visual Analogue Scale.;Tolerability of participants to the treatment assessed by Likert Scale.;Evaluate the clinical response assessed by the Visual Analogue Scale.;Evaluate the clinical response assessed by a questionnaire.
Secondary Outcome Measures
NameTimeMethod
Evaluate the sexual function of women with vulvodynia by Female Sexual Function Index (FSFI).;Evaluate the sexual function of women with vulvodynia by Sexual Quotient - Female Version (SQ-FV).
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