dyspareunie: Management of Women With Superficial Dyspareunia

Sponsor

Université de Reims Champagne-Ardenne (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT06142851

Collaborator

(none)

2,000

Enrollment

Locations

Anticipated Duration (Months)

1000

Patients Per Site

200.2

Patients Per Site Per Month

Study Details

Study Description

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.

Condition or Disease	Intervention/Treatment	Phase
Superficial Dyspareunia	Other: Data collection

Detailed Description

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

Study Design

Study Type:

Observational

Anticipated Enrollment :

2000 participants

Observational Model:

Case-Only

Time Perspective:

Cross-Sectional

Official Title:

Management of Women With Superficial Dyspareunia

Anticipated Study Start Date :

Dec 1, 2023

Anticipated Primary Completion Date :

Feb 1, 2024

Anticipated Study Completion Date :

May 1, 2024

Arms and Interventions

Arm	Intervention/Treatment
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 data collection

Arm

Intervention/Treatment

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

data collection

Outcome Measures

Primary Outcome Measures

medical history [Day 0]
Question to the woman about possible pain during sexual intercourses by an health professional (yes or no)

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

Female

Accepts 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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Ufr Medecine Urca	Reims		France	51100
2	Université de Reims Champagne Ardenne	Reims		France	51100

Sponsors and Collaborators

Université de Reims Champagne-Ardenne

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Université de Reims Champagne-Ardenne

ClinicalTrials.gov Identifier:

NCT06142851

Other Study ID Numbers:

2023_RIPH_017_PEC-dyspareunie

First Posted:

Nov 22, 2023

Last Update Posted:

Nov 22, 2023

Last Verified:

Nov 1, 2023

Individual Participant Data (IPD) Sharing Statement:

Undecided

Plan to Share IPD:

Undecided

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by Université de Reims Champagne-Ardenne

superficial dyspareunia

management

Additional relevant MeSH terms:

Dyspareunia

Study Results

No Results Posted as of Nov 22, 2023