Management of Women With Superficial Dyspareunia

NCT06142851 | Unknown

• 1 other identifier: 2023_RIPH_017_PEC-dyspareunie
• Study Type: observational
• Target: 2,000
• Locations: 1 country
• Sites: 2

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.

Conditions

Superficial Dyspareunia

Keywords

superficial dyspareunia; management

Outcome Measures

Primary Outcomes (1)

• medical history

  Question to the woman about possible pain during sexual intercourses by an health professional (yes or no)

  Day 0

Study Arms (1)

Women with superficial dyspareunia

Adult women, having sexual activity with or without vaginal penetration, suffering from superficial dyspareunia, whether or not managed by health professionals.

Other: Data collection

Interventions

Data collection OTHER

data collection

Women with superficial dyspareunia

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Women with superficial dyspareunia

You may qualify if:

• 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

You may not qualify if:

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

Sponsors & Collaborators

• Université de Reims Champagne-Ardenne: lead

Study Sites (2)

Ufr Medecine Urca

Reims, 51100, France

Location

Université de Reims Champagne Ardenne

Reims, 51100, France

Location

MeSH Terms

Interventions

Data Collection

Intervention Hierarchy (Ancestors)

Epidemiologic Methods; Investigative Techniques; Health Care Evaluation Mechanisms; Quality of Health Care; Health Care Quality, Access, and Evaluation; Public Health; Environment and Public Health

Central Study Contacts

Barbe Coralie, DR

CONTACT

0326913665; coralie.barbe@univ-reims.fr

CURRS CURRS

CONTACT

0326918822; currs@univ-reims.fr

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 15, 2023
• First Posted: November 22, 2023
• Study Start: December 1, 2023
• Primary Completion: February 1, 2024
• Study Completion: May 1, 2024
• Last Updated: November 22, 2023

Record last verified: 2023-11

Locations

FR (2)