Systemic Lupus Erythematosus (SLE) Clinical Trials

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Randomized Clinical Trial to Assess the Efficacy and Safety of a Primary Prevention Strategy for Cardiovascular Events in Patients With Inflammatory Rheumatic Diseases Based on the Use of Carotid Ultrasound

Status: Recruiting
Location: See all (17) locations...
Intervention Type: Other, Diagnostic test, Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

PREVENER is a randomized, open-label, multicenter, phase IV clinical trial designed to evaluate the efficacy and safety of a carotid ultrasound-based strategy for the primary prevention of cardiovascular events in patients with inflammatory rheumatic diseases (IRD). Patients with IRD, including rheumatoid arthritis (RA), psoriatic arthritis (PsA), axial spondyloarthritis (AxSpA), and systemic lupus erythematosus (SLE), have a 50% higher risk of cardiovascular (CV) events compared to the general population. However, conventional CV risk scores (SCORE2/OP) systematically underestimate this risk, leaving many high-risk patients without appropriate preventive treatment. Patients aged ≥50 years with IRD and low-to-moderate CV risk according to SCORE2/OP will be randomized 1:1 to either an experimental group (carotid ultrasound to detect subclinical atherosclerosis) or a control group (standard care according to ESC 2021 guidelines). Patients in the experimental group with carotid plaques will be reclassified as very high CV risk and treated with high-intensity statins (LDL target \<55 mg/dL). The primary endpoint is the incidence of major adverse cardiovascular events (MACE) over 48 months of follow-up.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: f
View:

• Patients aged ≥50 years who have provided written informed consent.

• Fulfillment of classification criteria for at least one of the following inflammatory rheumatic diseases:

‣ Rheumatoid arthritis (RA) according to ACR/EULAR 2010 criteria

⁃ Psoriatic arthritis (PsA) according to CASPAR criteria

⁃ Axial spondyloarthritis (AxSpA) according to ASAS criteria

⁃ Systemic lupus erythematosus (SLE) according to ACR/EULAR 2019 criteria

• Low-to-moderate cardiovascular risk according to SCORE2/OP classification.

Locations
Other Locations
Spain
Hospital General Universitario de Alicante
RECRUITING
Alicante
Hospital Universitario Vall d'Hebrón
RECRUITING
Barcelona
Hospital Universitario de Basurto
RECRUITING
Bilbao
Hospital General Universitario de Ciudad Real
NOT_YET_RECRUITING
Ciudad Real
Hospital Universitario Reina Sofía
NOT_YET_RECRUITING
Córdoba
Hospital Universitario de Elche
NOT_YET_RECRUITING
Elche
Hospital de Laredo
RECRUITING
Laredo
Hospital Universitario de Gran Canaria Dr. Negrín
NOT_YET_RECRUITING
Las Palmas De Gran Canaria
Hospital Universitario La Paz
NOT_YET_RECRUITING
Madrid
Hospital Universitario Ramón y Cajal
NOT_YET_RECRUITING
Madrid
Hispital Universitario Virgen de la Arrixaca
NOT_YET_RECRUITING
Murcia
Hospital Vega Baja de Orihuela
RECRUITING
Orihuela
Hospital Universitari Son LLàtzer
NOT_YET_RECRUITING
Palma
Hospital Universitario de Canarias
NOT_YET_RECRUITING
San Cristóbal De La Laguna
Hospital Universitario Marqués de Valdecilla
NOT_YET_RECRUITING
Santander
Hospital Sierrallana
RECRUITING
Torrelavega
Hospital Universitario Araba
RECRUITING
Vitoria-gasteiz
Time Frame
Start Date: 2026-04-22
Estimated Completion Date: 2031-12
Participants
Target number of participants: 1944
Treatments
Experimental: Experimental Group: Carotid Ultrasound
Patients undergo carotid ultrasound within 30 days of randomization. Patients with carotid plaques are reclassified as very high cardiovascular risk and initiated on high-intensity statin therapy (LDL target \< 55 mg/dL). Patients without carotid plaques are managed according to ESC 2021 guidelines.
Active_comparator: Control Group: Standard Care
Patients are managed according to standard ESC 2021 cardiovascular prevention guidelines throughout the study, without carotid ultrasound assessment.
Sponsors
Leads: Instituto de Investigación Marqués de Valdecilla

This content was sourced from clinicaltrials.gov