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Recruiting NCT06657846

NCT06657846 HRQoL and Financial Toxicity in Patients With VEXAS Syndrome

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Clinical Trial Summary
NCT ID NCT06657846
Status Recruiting
Phase
Sponsor Gruppo Italiano Malattie EMatologiche dell'Adulto
Condition VEXAS
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2024-11-01
Primary Completion 2025-06-10

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 99 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 100 participants in total. It began in 2024-11-01 with a primary completion date of 2025-06-10.

⚠ 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 multicenter cross-sectional observational study aims to describe health-related quality of life (HRQoL) and symptom profiles of patients with VEXAS syndrome.

Eligibility Criteria

Inclusion Criteria: * Adult patients (≥ 18 years old) with a confirmed diagnosis of VEXAS syndrome (UBA1 pathogenic mutation detected) * Written informed consent Exclusion Criteria: * \- Having any kind of psychiatric disorder or major cognitive dysfunction. * Not able to read and understand local language

Contact & Investigator

Central Contact

Fabio Efficace

✉ f.efficace@gimema.it

📞 +39 06 441639831

Frequently Asked Questions

Who can join the NCT06657846 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 99 Years, studying VEXAS. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06657846 currently recruiting?

Yes, NCT06657846 is actively recruiting participants. Contact the research team at f.efficace@gimema.it for enrollment information.

Where is the NCT06657846 trial being conducted?

This trial is being conducted at Ancona, Italy, Bergamo, Italy, Bologna, Italy, Brescia, Italy and 11 additional locations.

Who is sponsoring the NCT06657846 clinical trial?

NCT06657846 is sponsored by Gruppo Italiano Malattie EMatologiche dell'Adulto. The trial plans to enroll 100 participants.

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