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Act on Quality of Life in Patients With aortIc Stenosis

Act on Quality of Life in Poor Prognosis Aortic Stenosis Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06477042
Acronym
ALPINIST
Enrollment
240
Registered
2024-06-27
Start date
2024-12-19
Completion date
2027-12-19
Last updated
2025-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe Aortic Stenosis

Keywords

TAVI, quality of life, Aortic Stenosis

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).

Interventions

OTHERKansas City Cardiomyopathy Questionnaire (KCCQ-12) score

Change in quality-of-life score assessed by the Kansas City Cardiomyopathy Questionnaire (KCCQ-12) between the 2-month early visit and inclusion in the poor-prognosis group.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Kansas City Cardiomyopathy Questionnaire (KCCQ-12) score variation between the 2-months visit and inclusion.Day 0 and Month 2Change in quality-of-life score assessed by the Kansas City Cardiomyopathy Questionnaire (KCCQ-12) between the 2-month early visit and inclusion in the poor-prognosis group. The KCCQ-12 contains four subdomains: Physical Limitation, Symptom Frequency, Quality of Life, and Social Limitations. Each subdomain provides an individual score from 0 to 100, with 0 denoting the worst and 100 the best possible health status

Countries

France

Contacts

Primary ContactPierre Lantelme, MD
pierre.lantelme@chu-lyon.fr04.72.07.25.36
Backup ContactJulia Canterini
Julia.canterini@chu-lyon.fr04 27 85 66 28

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026