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Management of Women With Superficial Dyspareunia

Management of Women With Superficial Dyspareunia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06142851
Acronym
dyspareunie
Enrollment
2000
Registered
2023-11-22
Start date
2023-12-01
Completion date
2024-05-01
Last updated
2023-11-22

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

Conditions

Superficial Dyspareunia

Keywords

superficial dyspareunia, management

Brief summary

Superficial dyspareunia are persistent or recurrent pains during an attempt at sexual intercourse or during effective penetration. They affect between 3 to 18% of women and are a source of physical and psychological suffering. Some health professionals (gynecologists, general practitioners, midwives) are confronted daily with these complaints. The approach of sexuality remains a complex subject even within the medical field. As a result, communication between women and health professionals can be difficult, leading to delayed diagnosis or inadequate management.

Detailed description

The main objective is to describe the management of superficial dyspareunia by health professionals.

Interventions

OTHERData collection

data collection

Sponsors

Université de Reims Champagne-Ardenne
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged 18 or over * Superficial dyspareunia, i.e.: * Having already had several painful vaginal penetrative sex * Having pain at the intromission (at the beginning of the vagina and at the level of the vulva) and/or at the beginning of penetration (by a penis, fingers, sextoys) * Having persistent and/or recurrent pain (appearing in a manner regular) * Agreeing to participate in the study

Exclusion criteria

* Minors * Protected by law (guardianship, curatorship, safeguarding of justice) * Refusing to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
medical historyDay 0Question to the woman about possible pain during sexual intercourses by an health professional (yes or no)

Countries

France

Contacts

Primary ContactBarbe Coralie, DR
coralie.barbe@univ-reims.fr0326913665
Backup ContactCURRS CURRS
currs@univ-reims.fr0326918822

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026