Screening for fibromyalgia in women with suspected endometriosis

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This single-center prospective cohort will invite all women presenting for an initial visit to the Assuta Ashdod endometriosis clinic to complete validated fibromyalgia questionnaires, including the Modified ACR Preliminary Diagnostic Criteria, before their appointment. Researchers will determine the prevalence of fibromyalgia among patients with suspected endometriosis, stage endometriosis using the AAGL classification, and correlate fibromyalgia diagnoses with ultrasound and surgical findings. The study excludes women with a prior fibromyalgia diagnosis and will compare symptom changes in patients diagnosed with both conditions versus those with only one. No therapeutic interventions are provided as part of this observational protocol.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* All women with suspected endometriosis in their first visit to endometriosis clinics in Assuta Ashdod Hospital

Exclusion Criteria:

* Proven fibromyalgia prior to the first visit.

Where it's running

• Assuta Ashdod University Hospital
  Ashdod, Israel Recruiting

Study contacts

• Study coordinator: Oshri Barel, MD
• Email: oshrib@assuta.co.il
• Phone: +972559382117

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Imaging endometriosis with a special PET tracer in adult women

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• Fiber supplement for digestive symptoms in endometriosis

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.