About this trial
This observational study aims at establishing the proportion of patients suffering from endometriosis and for whom an Obstructive Sleep Apnea Hypopnea Syndrome (OSAHS) diagnosis is established.
The study participation will be offered to endometriosis patients displaying symptoms that may suggest an underlying OSAHS.
OSAHS diagnosis will be made according to standard of care practice and patients will be followed up to 12 months after initiating the OSAHS treatment to fill in questionnaires assessing the impact of OSAHS treatment on various endometriosis-related symptoms
Eligibility criteria
Qualifiers
Female patients aged between 18 and 50 years of age
Confirmed diagnostic of endometriosis (either through imaging procedure (ultrasound or RMI) or diagnostic coelioscopy)
Patient suffering from symptoms evocating Obstructive Sleep Apnea Hypopnea Syndrome (OSAHS) and justifying a diagnosis process performed within Standard of Care practice
Patient who has been informed about the study and has signed the informed consent form prior to any study-specific procedures
Disqualifiers
Post menopausal patient
Ongoing treatment for OSAHS
Patient with Chronic Obstructive Pulmonary Disease (COPD) or unstabilized cardiac disorders
Concomitant participation in another clinical trial
Trial design
Treatments tested in this trial
- questionnaires completion