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Clinical Trial ● Currently Recruiting NCT06047561

The Scottish Aortic Stenosis LongiTudinal Imaging and biomarkeR (SALTIRE) Programme

The Scottish Aortic Stenosis LongiTudinal Imaging and biomarkeR (SALTIRE) Programme — Recruiting • Cardiology / Cardiovascular • NCT06047561.

📅 21 Sep 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
NCT ID
NCT06047561
Sponsor
University of Edinburgh
Start
2023-05-22
ClinicaliQ Trial Snapshot
  • The Scottish Aortic Stenosis LongiTudinal Imaging and biomarkeR (SALTIRE) Programme — Recruiting • Cardiology / Cardiovascular • NCT06047561.
  • What is being tested: SALTIRE is investigating the underlying mechanisms driving aortic stenosis progression and post-valve replacement outcomes through longitudinal imaging (echocardiography every 6 months) combined with biomarker analysis to identify disease accelerators and predictive factors.
  • Patient eligibility overview: The study recruits patients across the aortic stenosis disease spectrum, including those with asymptomatic or symptomatic disease at various stages of severity, as well as patients who have undergone aortic valve replacement, enabling comparison across disease trajectory.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The goal of this observational study is to understand the processes of what causes and accelerates the disease progress in aortic stenosis and following aortic valve replacement. Participants will undergo transthoracic echocardiography every 6 months, with annual visits for state-of-the-art scanning techniques including positron-emission tomography combined with computed tomography or magnetic resonance imaging with radiotracers designed to look at disease processes including fibrosis, calcification, inflammation and thrombosis activity.

Eligibility Snapshot
  • : * Male or female aged >50 years * Provision of informed consent prior to any study specific procedures * Patients with bioprosthetic aortic valve replacements, including both surgically and transcatheter implanted valves * Patients with severe aortic stenosis (peak velocity >4.0 m/s; previously recruited patients) * Patients with moderate aortic stenosis (peak velocity 3.0-4.0 m/s; new prospectively recruited patients) * Patients with mild aortic stenosis (peak velocity 2.5-2.9 m/s; new prospectively recruited patients) * Patients with aortic sclerosis (tri-leaflet thickened aortic valve with no obstruction of ventricular outflow) * Age and sex-matched healthy volunteers

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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