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Recruiting NCT06477042

NCT06477042 Act on Quality of Life in Patients With aortIc Stenosis

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Clinical Trial Summary
NCT ID NCT06477042
Status Recruiting
Phase
Sponsor Hospices Civils de Lyon
Condition Severe Aortic Stenosis
Study Type OBSERVATIONAL
Enrollment 240 participants
Start Date 2024-12-19
Primary Completion 2027-12-19

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Kansas City Cardiomyopathy Questionnaire (KCCQ-12) score

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 240 participants in total. It began in 2024-12-19 with a primary completion date of 2027-12-19.

⚠ 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

Aortic stenosis (AS) is a degenerative process affecting the aortic valve that leads to sclerosis of the valve and limits its opening during cardiac contractions. The prognosis is poorly, with survival rates of only 15-50% at 5 years. AS has a major impact on quality of life, with severely limiting symptoms (dyspnea, chest pain,…) often leading to repeated hospitalizations. It is the most common valvular disease in Europe and North America, and its prevalence is increasing as the population ages. In Europe, 17% of the population is aged 65 or over; in France, this proportion will reach 30% by 2030, corresponding to 16 million people. The incidence of aortic valve sclerosis (early stage AS) is around 25% at age 65, rising to 48% after age 75. The prevalence of aortic valve disease is likely to continue to rise, given the expected evolution of the age pyramid. There is no medical treatment able to slow down the degenerative process of the valve, and the only treatment is aortic valve replacement when the AS becomes constricted and the patient is eligible for an intervention. Aortic valve replacement has historically been performed surgically, with open-chest surgery to remove the damaged valve and replace it with a mechanical or biological valve prosthesis. Now Transcatheter Aortic Valve Implantation (TAVI) has replaced this procedure. This involves inserting a bioprosthesis crimped into a stent via an endovascular route, i.e. without opening the thorax. Deployment of the stent crushes the native valve, leaving the functional bioprosthesis in place. Initially developed for patients contraindicated to surgery, TAVI is now offered as a first-line treatment for patients aged 75 and over. Inexistent before 2010, the number of TAVIs equalled the number of surgeries by 2015, and TAVIs currently account for ¾ of aortic valve procedures (unpublished data).

Eligibility Criteria

Inclusion Criteria: * Patients with symptomatic aortic stenosis (exertional dyspnea, angina, malaise/syncope) * Indication for TAVI (valve area 1 cm² or 1 cm²/m² body surface area or mean transvalvular aortic gradient \> 40 mmHg on ultrasound) validated in Heart Team * Charlson score ≥ 5 * Social health care insurance affiliation Exclusion Criteria: * Patient refusing TAVI procedure * CT scan not performed during the pre-TAVI assessment * Patient unable to understand or answer quality-of-life questionnaires * Pregnant or breast-feeding women * Patients participating in other interventional research that may interfere with the present study with an exclusion period still in progress * Persons under judicial protection * Patients under guardianship, curators or safeguard of justice

Contact & Investigator

Central Contact

Pierre Lantelme, MD

✉ pierre.lantelme@chu-lyon.fr

📞 04.72.07.25.36

Frequently Asked Questions

Who can join the NCT06477042 clinical trial?

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

Is NCT06477042 currently recruiting?

Yes, NCT06477042 is actively recruiting participants. Contact the research team at pierre.lantelme@chu-lyon.fr for enrollment information.

Where is the NCT06477042 trial being conducted?

This trial is being conducted at Clermont-Ferrand, France, Lille, France, Lyon, France, Nantes, France.

Who is sponsoring the NCT06477042 clinical trial?

NCT06477042 is sponsored by Hospices Civils de Lyon. The trial plans to enroll 240 participants.

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