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Evaluation of Prevalence of Sexuality Alteration in Women With an Abnormal Pap Test — EVASEF  

Sexual Dysfunction Clinical Trial

Official title:
Evaluation of Prevalence of Sexuality Alteration in Women With an Abnormal Pap Test

Clinical Trial Summary

Human Papilloma virus is the most common sexual infection in women, which can leads to cervical lesion and cervical cancer. Pap test is recommanded in women of 25 years old until 65 years old in order to screen subclinic lesions and improve prognosis. Yet, scientific knowledge about chronic disease showed negative consequences on quality of life. However, no study until now has striven to evaluate the consequences of an abnormal pap test on sexuality in adult women. The aim of this study is to evaluate if an abnormal pap test have an impact on the sexual functions in women because of the anxiety and psychological consequences of the diagnosis

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05701020
Study type Interventional
Source Centre Hospitalier Universitaire, Amiens
Contact
Status Completed
Phase N/A
Start date December 13, 2022
Completion date September 12, 2023
View Details
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