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Clinical Trials in Italy / NCT06773065
Recruiting Observational

Central Awareness in Women With Endometriosis

NCT06773065 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2022-01-14
Last updated
2025-01-14

Condition(s) studied

Endometriosis

Study summary

Gathering some information obtained during the gynaecological examination and transvaginal ultrasound check-up to be able to assess the prevalence of Central Sensitisation Syndrome (CSS) in women with endometriosis and also to be able to assess related risk factors. CSS has been defined as an algic syndrome due to a hyperactivation of the sensitivity circuit at a central level; the diagnosis is based on the result obtained from a questionnaire, the Central Sensitisation Inventory (CSI), which evaluates the presence and intensity of 25 clinical symptoms. For this reason, a questionnaire is proposed to be completed at the time of the check-up visit.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * Women with a clinical, ultrasound and/or surgical diagnosis of endometriosis * Aged between 18 and 50 years * Patients starting or already taking hormone therapy * Patients coming for a first visit or outpatient follow-up visit * Signature of informed consent to participate in the study Exclusion Criteria: * Post-menopausal women (spontaneous or iatrogenic) * Virgo patients * Patients with poor compliance with hormone therapy, who are not taking it properly or have discontinued therapy spontaneously * Positive history of any malignant neoplasm * Positive medical history of specific medical conditions that adversely affect the central nervous system, such as: brain or spinal cord damage, neurological diseases or peripheral nerve damage, multiple sclerosis

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna Italy Recruiting

More IRCCS Azienda Ospedaliero-Universitaria di Bologna trials in Italy

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06773065 on ClinicalTrials.gov ↗ ← All trials in Italy