← Back to Clinical Trials
Recruiting NCT07483853

NCT07483853 Reliability and Validation of the WB-MRI Radiological Score in CRMO

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07483853
Status Recruiting
Phase
Sponsor IRCCS Azienda Ospedaliero-Universitaria di Bologna
Condition Chronic Recurrent Multifocal Osteomyelitis
Study Type OBSERVATIONAL
Enrollment 15 participants
Start Date 2027-01-01
Primary Completion 2027-04-01

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age 32 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 15 participants in total. It began in 2027-01-01 with a primary completion date of 2027-04-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study evaluates the inter-observer reliability of a standardized WB-MRI scoring system for CRMO and its consistency with the PedCNO clinical score. It also investigates whether changes in the radiologic score mirror therapeutic response, supporting a more objective clinical-radiological disease assessment.

Eligibility Criteria

Inclusion Criteria: * Patients with a diagnosis of CRMO according to the international Bristol clinical and radiologic criteria, followed at the Pediatric Rheumatology Clinic of the Pediatric Unit, IRCCS AOU Bologna, Sant'Orsola Hospital; * Age under 18 years at the time of CRMO diagnosis; * At least one WB-MRI performed as part of routine clinical follow-up between January 2015 and the start date of the study; * Availability of complete clinical documentation (including reports, radiologic images, and clinical information) sufficient to apply both the WB-MRI score and the PedCNO score; * Obtain informed consent. Exclusion Criteria: \- Alternative diagnoses accounting for the bone lesions (e.g., infections, neoplasms).

Contact & Investigator

Central Contact

Angela Miniaci

✉ angela.miniaci@aosp.bo.it

📞 00390512144811

Frequently Asked Questions

Who can join the NCT07483853 clinical trial?

This trial is open to participants of all sexes, up to 32 Years, studying Chronic Recurrent Multifocal Osteomyelitis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07483853 currently recruiting?

Yes, NCT07483853 is actively recruiting participants. Contact the research team at angela.miniaci@aosp.bo.it for enrollment information.

Where is the NCT07483853 trial being conducted?

This trial is being conducted at Bologna, Italy.

Who is sponsoring the NCT07483853 clinical trial?

NCT07483853 is sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. The trial plans to enroll 15 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology