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Recruiting NCT06735001

NCT06735001 Identification of the Metabolic Signature of Atrial Fibrillation for Personalized Prevention

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Clinical Trial Summary
NCT ID NCT06735001
Status Recruiting
Phase
Sponsor University Hospital, Bordeaux
Condition Atrial Fibrillation (AF)
Study Type INTERVENTIONAL
Enrollment 400 participants
Start Date 2025-03-10
Primary Completion 2029-10

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
FA ablationLab test

Eligibility Fast-Check

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

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 400 participants in total. It began in 2025-03-10 with a primary completion date of 2029-10.

⚠ 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

Atrial fibrillation (AF) is a major public health problem. The efficacy of the existing techniques is limited in the more aggressive forms. It is therefore necessary to develop approaches, in particular the identification of relevant biomarkers, to prevent the onset, recurrence or progression of AF in at-risk patients. The objective of this study is to describe the longitudinal metabolic and biomolecular signature of AF in patients eligible for cardiac ablation.

Eligibility Criteria

Inclusion Criteria: * Age ≥ 18 years, all genders, and ethnic origins * Free, informed, and written consent signed * Person affiliated to or benefiting from a social security scheme Exclusion Criteria: * Age \< 18 years * Lack of informed consent * Gestating women (pregnancy test carried out as part of care for FA patients, contraception, or menopause for women in control groups) * Persons under administrative or judicial protection * Endocarditis or pericarditis in progress or within the 3 last months * Active tumor pathology (benign or malignant) * Chronic inflammation or autoimmune disease * Chronic liver disease * Myocardial infarction within the last 8 weeks

Contact & Investigator

Central Contact

Guido CALUORI

✉ guido.caluori@ihu-liryc.fr

📞 +33 5 35 38 19 58

Principal Investigator

Nicolas DERVAL

PRINCIPAL INVESTIGATOR

University Hospital, Bordeaux

Frequently Asked Questions

Who can join the NCT06735001 clinical trial?

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

Is NCT06735001 currently recruiting?

Yes, NCT06735001 is actively recruiting participants. Contact the research team at guido.caluori@ihu-liryc.fr for enrollment information.

Where is the NCT06735001 trial being conducted?

This trial is being conducted at Pessac, France.

Who is sponsoring the NCT06735001 clinical trial?

NCT06735001 is sponsored by University Hospital, Bordeaux. The principal investigator is Nicolas DERVAL at University Hospital, Bordeaux. The trial plans to enroll 400 participants.

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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