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Recruiting NCT07563660

NCT07563660 FAPI PET/CT Imaging in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) (FAPI-ARVC))

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Clinical Trial Summary
NCT ID NCT07563660
Status Recruiting
Phase
Sponsor Istanbul University - Cerrahpasa
Condition Arrhythmogenic Right Ventricular Cardiomyopathy
Study Type INTERVENTIONAL
Enrollment 15 participants
Start Date 2025-04-16
Primary Completion 2026-08-25

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
68Ga-DOTA-SA-FAPI PET/CT

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 15 participants in total. It began in 2025-04-16 with a primary completion date of 2026-08-25.

⚠ 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

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease associated with fibrofatty myocardial replacement, ventricular arrhythmias, and an increased risk of sudden cardiac death. Although current diagnostic approaches, including the 2010 Task Force Criteria and the Padua criteria, improve recognition of the disease, early diagnosis remains challenging, particularly when structural abnormalities are subtle or absent on conventional imaging. Echocardiography and cardiac magnetic resonance imaging are central to evaluation, but their sensitivity for early or active fibrotic remodeling may be limited. This limitation may be particularly relevant in patients who are unable to undergo cardiac magnetic resonance imaging, in whom 68Ga-DOTA-SA-FAPI PET/CT may provide complementary diagnostic information. This prospective single-group diagnostic imaging study aims to investigate the incremental value of protocol-specified 68Ga-DOTA-SA-FAPI PET/CT imaging in patients with ARVC. FAPI PET/CT is a novel molecular imaging method that targets activated fibroblasts and may allow non-invasive detection of active myocardial fibrosis.Fifteen adult patients with an established diagnosis of ARVC will undergo protocol-specified 68Ga-DOTA-SA-FAPI PET/CT imaging in addition to clinical evaluation, electrocardiography, echocardiography, and review of previously obtained cardiac magnetic resonance imaging findings. FAPI PET/CT findings will be compared with conventional diagnostic criteria and other clinical and imaging parameters, including previously available cardiac magnetic resonance imaging findings. Participants will also be followed clinically for 6 months after imaging to explore possible associations between FAPI uptake and short-term clinical outcomes, including arrhythmic events, ventricular function, and laboratory markers. The study is expected to provide preliminary evidence on whether 68Ga-DOTA-SA-FAPI PET/CT may improve the detection of myocardial fibrosis and contribute to diagnostic assessment and risk stratification in ARVC. It may also help clarify the potential role of FAPI PET/CT in patients who are unable to undergo cardiac magnetic resonance imaging. The findings may support future larger prospective studies in this field.

Eligibility Criteria

Inclusion Criteria: * Adults aged 18 years or older * Established diagnosis of arrhythmogenic right ventricular cardiomyopathy according to the 2010 Revised Task Force Criteria and/or the Padua criteria * Under active follow-up at the study center * Ability to understand the study procedures and provide written informed consent Exclusion Criteria: * History of malignancy * Severe renal impairment * Severe hepatic impairment * Pregnancy or breastfeeding * Prior 68Ga-DOTA-SA-FAPI PET/CT imaging * Inability or unwillingness to provide written informed consent * Any medical, clinical, or logistical condition that, in the opinion of the investigators, could interfere with study participation, image interpretation, or completion of follow-up

Contact & Investigator

Central Contact

Sukru Arslan, MD, Associate Professor

✉ sukru.arslan@iuc.edu.tr

📞 +90 555 623 2606

Frequently Asked Questions

Who can join the NCT07563660 clinical trial?

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

Is NCT07563660 currently recruiting?

Yes, NCT07563660 is actively recruiting participants. Contact the research team at sukru.arslan@iuc.edu.tr for enrollment information.

Where is the NCT07563660 trial being conducted?

This trial is being conducted at Istanbul, Turkey (Türkiye).

Who is sponsoring the NCT07563660 clinical trial?

NCT07563660 is sponsored by Istanbul University - Cerrahpasa. The trial plans to enroll 15 participants.

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