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Study identifier: NCT06773065 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Central Awareness in Women With Endometriosis

Condition: Endometriosis  ·  Sponsor: IRCCS Azienda Ospedaliero-Universitaria di Bologna

PhaseN/A
Planned participants310
Who can joinFemale, 18 Years to 50 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Diego Raimondo, MD  ·  +393290636618  ·  die.raimondo@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

IRCCS Azienda Ospedaliero-Universitaria di BolognaBologna, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06773065