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The effect of Vaginal Dilator and Perineal Massage techniques in women with sexual pain

Effect of adding Vaginal Dilators to the Perineal Massage technique in women with Genito-Pelvic/Penetration pain: randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-96d7ym7
Enrollment
Unknown
Registered
2023-10-11
Start date
2023-09-08
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dyspareunia

Interventions

E02.190.599
This is a parallel randomized controlled trial study (1:1 ratio), blind, with hidden allocation. The participants evaluated will be randomly divided into two groups, group A being 31 participants in m

Sponsors

Faculdade de Educação Física e Fisioterapia - Universidade Federal de Uberlândia
Lead Sponsor
Faculdade de Educação Física e Fisioterapia - Universidade Federal de Uberlândia
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Women over 18 years of age; who have had sexual intercourse with vaginal penetration; who have genito-pelvic/penetration pain disorder before during or after sexual intercourse

Exclusion criteria

Exclusion criteria: Women who do not tolerate the introduction of a finger into the vaginal introitus; pregnant women; pelvic inflammatory disease; women after pelvic radiotherapy

Design outcomes

Primary

MeasureTime frame
Evaluating pain during sexual intercourse verified by Analogic Visual Scale and presenting the parameters in numbers we will observe the reduction in sexual pain—

Secondary

MeasureTime frame
Evaluating the sexual function verified by the Female Sexual Function Index and presenting the parameters in numbers we will observe the increase in sexual satisfaction—

Countries

Brazil

Contacts

Public ContactLyana Marinho

Universidade Federal de Uberlândia

lyanamarinho8@gmail.com+55(34)3239-4411

Outcome results

None listed

Source: REBEC (via WHO ICTRP)