Central Awareness in Women With Endometriosis
Recruiting
Observational Study
Endometriosis
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 50
- Sex
- Female
- Study type
- Observational
- Participants needed
- 310 (estimated)
- Sponsor
- IRCCS Azienda Ospedaliero-Universitaria di Bologna · Other
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About This Trial
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 ba…
Trial Locations
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Eligibility Criteria
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…
Contacts