NCT06773065Recruiting
Central Awareness in Women With Endometriosis
The Role Of Central Sensitisation In Women With Endometriosis: A Prospective Observational Study
Source: ClinicalTrials.gov · Last updated 14 Jan 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 310 (estimated)
- First submitted
- 1 Dec 2024
- Start date
- 14 Jan 2022
- Primary completion date
- 31 Jan 2025
- Lead sponsor
- IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Diseases
- Endometriosis
- NCT number
- NCT06773065
What you commit to
- Study type: Observational
- Planned participants: 310
- From 14 Jan 2022 to the primary completion date, 31 Jan 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with poor compliance with hormone therapy, who are not taking it properly or have discontinued therapy spontaneously
Other illness
- 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
Other
- Post-menopausal women (spontaneous or iatrogenic)
- Virgo patients
Who the study is looking for
- 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
Age in the registry: 18 years to 50 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna Coordinator of this site? Confirm its status | Bologna | Italy | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.