Impact of Ehlers-Danlos Syndrome on Gynaecological Health
ConditionEhlers-Danlos Syndrome (EDS)
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-50
SponsorUniversity Hospital, Rouen
About this trial
Dysmenorrhea is a common problem in gynaecology, significantly impacting patients' quality of life. Ehlers-Danlos syndrome (EDS) is associated with joint hypermobility, tissue fragility and chronic pain. Some studies suggest an increased prevalence of gynaecological disorders, including dysmenorrhea, in patients with EDS. However, data remain limited and few studies have compared the intensity and characteristics of dysmenorrhea in women with EDS. There is also little data on the prevalence of other gynaecological conditions in women with EDS.
This study therefore aims to compare the severity of dysmenorrhea in patients with EDS and a control group in order to better characterise the gynaecological impact of EDS. It will also compare the prevalence of other gynaecological conditions between women with EDS and women without EDS.
Eligibility criteria
Qualifiers
Women aged 18 or over.
Willing to participate voluntarily in the study via an online questionnaire.
Of childbearing age.
Reporting a diagnosis of EDS (all types) or not having EDS (control group) and being part of a database of healthy volunteers.
Disqualifiers
Minors (< 18 years old).
Menopausal women
People who do not understand French well enough to complete the questionnaire.
Uncertain diagnosis of EDS (exclusion of participants who suspect EDS but without medical confirmation).
Trial design
Treatments tested in this trial
- Not listed
Trial groups
156 Participants
are grouped into 2 trial groupsSponsors and collaborators
Source ClinicalTrials.gov