The Early Detection and Progression of Subclinical Atherosclerosis in Psoriasis
NCT ID: NCT05858099
Last Updated: 2023-09-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
120 participants
OBSERVATIONAL
2020-01-30
2030-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
* To assess the prevalence, vascular distribution and burden of subclinical atherosclerosis in patients with psoriasis and its relationship with inflammatory biomarkers and cardiovascular (CV) risk algorithms using 2D vascular ultrasound (2DVUS) of carotid and femoral arteries, 3D vascular ultrasound (3DVUS) of carotid and femoral arteries and Coronary Computed Tomography Angiography (CCTA).
* To characterize the composition of atherosclerotic plaques by CCTA and 3DVUS of the carotid and femoral arteries.
* To evaluate the effect of different treatments used in psoriasis on the progression and characterisation of subclinical atherosclerosis in different arterial territories assessed by non-invasive imaging techniques.
* To characterise the atherosclerosis process in patients with psoriasis using laboratory analysis and "-omics" technologies, as well as to evaluate changes at the molecular level after treatment of the skin disease.
Participants will undergo 2 study visits:
* At baseline, before starting biologic treatment for psoriasis. A 1-year follow up, after having completed one year under biologic treatment for psoriasis.
* Both visits include a clinical interview, physical examination, fasting blood draw and assessment of atherosclerotic disease by non-invasive vascular imaging tests (2D/3DVUS and CCTA).
* Participants may undergo an unscheduled clinical visit if the patient suffers a worsening of the psoriasis. This visit includes a clinical interview, physical examination and fasting blood draw.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Psoriasis and the Risk of Cardiovascular Disease. A Prospective Study
NCT01382784
Risk Indicators of Sarcoidosis Evolution-Unified Protocol
NCT05567133
Study of Molecular Markers in Cutaneous Inflammation Between Psoriatic Lesional Skin and Healthy Non-lesional Skin
NCT03423004
Identification of Cutaneous and Blood Biomarkers Predictive of Response to Systemic Treatments During Chronic Inflammatory Skin Diseases
NCT06599411
A Protocol Based Treatment for Debilitating Fibrosing Skin Disorders With (Anti-CD 20), Rituximab, Evaluating Safety and Efficacy
NCT00936546
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Psoriasis patients aged between 30 to 65 years.
Exclusion Criteria
* Patients undergoing oncological treatment.
* History of transplantation with active immunosuppressive or immunomodulatory treatment.
* Patients with morbid obesity (body mass index ≥40 kg/m2).
* Patients with diabetes mellitus.
* Patients with chronic liver disease.
* Patients with chronic kidney disease (glomerular filtration rate \<60 mL/min/1.73 m2).
* Patients with other chronic inflammatory disease, presence of any pathology that decreases life expectancy to less than 3 years, or any disease or condition that could affect adherence to study procedures.
* Patients that have had a chest computed tomography scan in the previous year.
* Pregnant or breastfeeding women.
30 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
HM Sanchinarro University Hospital
OTHER
Hospital Universitario 12 de Octubre
OTHER
Medstar Health Research Institute
OTHER
Hospital Nacional de Parapléjicos de Toledo
OTHER
Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Alvaro Gonzalez Cantero
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Álvaro González Cantero, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Fundación Hospital Ramón y Cajal
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ramón y Cajal University Hospital
Madrid, , Spain
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Abbad-Jaime de Aragon C, Berna-Rico E, Ballester-Martinez MA, Jaen P, Solis J, Barderas MG, Fernandez-Friera L, N Mehta N, Gelfand JM, Gonzalez-Cantero A. Early Detection and Progression of Subclinical Atherosclerosis in Psoriasis (EDSAP): protocol for an observational, single-centre, prospective cohort study. BMJ Open. 2023 Sep 26;13(9):e072455. doi: 10.1136/bmjopen-2023-072455.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CI-BIOB-058-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.