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NCT Number: NCT07472049

Symptomatic and Systemic Atherosclerotic Plaque Activity in Patients With Peripheral Arterial Disease Using Novel Imaging

The goal of this observational study is to characterise the relationships between inflammation, microcalcification and thrombus activity in atherosclerotic plaques in peripheral and systemic vascular territories in patients with symptomatic peripheral arterial disease.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Royal Infirmary of Edinburgh

Edinburgh, Midlothian, EH16 4SA, United Kingdom

Location status: Recruiting

Location contact

Allison C Winarski, MBChB MRCS (Ed)

SUB_INVESTIGATOR

Allison C Winarski, MBChB MRSC(Ed)

CONTACT

[email protected]

+447495905258

David E Newby, BSc (Hons)PhD BM DM DSc FRCP

SUB_INVESTIGATOR

Rachael O Forsythe, MBChB, PhD, FRCS (Vascular)

CONTACT

[email protected]

01312423585

Rachael O Forsythe, MBChB, PhD, FRCS (Vascular)

PRINCIPAL_INVESTIGATOR

About this study

In peripheral arterial disease (PAD), arteries in the lower body can become narrowed and develop blockages due to a process called atherosclerosis, leading to reduced blood flow to the lower limbs. Symptoms can range from mild cramping pain in legs on walking, to loss of parts of the leg. Patients with PAD are also at a high risk of blockages in other arteries in the body that can lead to problems such as heart attacks and strokes. Despite improvements in medical treatments and surgery, the outlook for patients with PAD has not improved.

Further information is required to understand the relationships between the processes that lead to narrowing and blockages (atherosclerosis) of the arteries and if they behave the same in different parts of the body. This can help to identify targeted treatments to reduce the risk of the disease getting worse and avoid heart attacks and strokes.

In this study investigators plan to recruit 100 people with symptomatic PAD to undergo a series of whole body PET-CT and CT angiogram scans using different tracers targeting the processes involved in atherosclerosis. Investigators will aim to co-enrol patients taking part in the LEADER-PAD study (NCT04774159).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female aged > 18 years
  • Symptomatic atherosclerotic peripheral artery disease;
  • Intermittent claudication; with ankle/arm blood pressure ratio <0.90 or artery stenosis >50% in addition to at least one of the following;
  • >1 vascular bed affected by atherosclerosis
  • Diabetes
  • Heart failure
  • Chronic kidney disease (eGFR < 60 mL/min/1.73 m2)
  • Rest pain or necrosis of limb or gangrene of limb
  • Revascularization defined as limb bypass surgery or endovascular revascularization procedures (irrespective of the specific device used), including percutaneous transluminal angioplasty/stent of iliac or infra-inguinal arteries or extra-anatomical bypass surgery
  • Leg or foot amputation for arterial vascular indications
  • Ability to give written or verbal informed consent

Exclusion criteria

  • Contraindication to colchicine or iodinated contrast
  • Long term requirement for colchicine for another clinical indication
  • Active diarrhoea
  • Recent lower limb revascularisation for symptomatic disease (<6 weeks)
  • Renal failure (glomerular filtration rate <30 mL/min/1.73 m2)
  • Cirrhosis or severe chronic liver disease
  • Women who are pregnant or breast-feeding
  • Women of child-bearing potential not protected by reliable contraception or is planning conception during the study
  • Current or planned long term use of cyclosporine, verapamil, HIV protease inhibitors, azole antifungals, or macrolide antibiotics (apart from azithromycin)
  • Patients deemed unlikely to return for follow up
  • Life expectancy <1 year
  • Inability or unwilling to give informed consent

Treatment and study plan

Whole body [68Ga]DOTATATE PET-CT

Radiation

Targeting vascular inflammation

Whole body [18F]GP1 PET-CT

Radiation

Targeting thrombus activity

Whole body [18F]NaF PET-CT

Radiation

Targeting vascular microcalcification

Whole body CT angiogram

Radiation

To determine anatomical and morphological atherosclerotic plaque characteristics

Primary outcomes

  1. Quantification of PET tracer uptake of [68Ga]DOTATATE, [18F]GP1 and [18F]NaF in the symptomatic lower limb(s)

    Time frame: From baseline imaging until completion imaging at 1 year

    The 3 primary endpoints will be the location and degree of:

    • inflammation: uptake of [68Ga]DOTATATE
    • calcification: uptake of [18F]NaF
    • thrombus activity: uptake of [18F]GP1 in peripheral arterial disease affecting the lower limbs. This will be determined by the degree of tracer standardised uptake values (SUVs) at the site of the symptomatic atherosclerotic plaque.

Secondary outcomes

  1. Quantification of PET tracer uptake of [68Ga]DOTATATE, [18F]GP1 and [18F]NaF in remote arterial territories

    Time frame: From baseline imaging until completion imaging at 1 year

    The secondary outcome measures will be the location and degree of inflammation, calcification and thrombus activity in remote arterial territories, including the coronary arteries, cerebral arteries, aorta and mesenteric vessels, as determined by SUVs of [68Ga]DOTATATE, [18F]NaF and [18F]GP1, respectively.

  2. CT plaque morphology

    Time frame: From baseline imaging to completion imaging at 1 year

    Investigators will characterise CT plaque morphology (total, calcified, non-calcified and low-attenuation plaque) in peripheral and systemic arterial beds and compare this to areas of [68Ga]DOTATATE, [18F]GP1 and [18F]NaF uptake.

  3. The association between patient risk factors for cardiovascular disease and PET tracer uptake

    Time frame: Frome baseline imaging to completion imaging at 1 year

    Investigators will explore the association between patient risk factors for cardiovascular disease (hypertension, diabetes, smoking) and the degree of [68Ga]DOTATATE, [18F]GP1 and [18F]NaF uptake as quantified by standard uptake values (SUVs). This will be measured by odds ratio (OR) with 95% confidence interval (CI) for each risk factor-tracer combination.

  4. The progression of microcalcification, as defined by [18F]NaF uptake, to macrocalcification.

    Time frame: From baseline imaging to completion imaging at 1 year

    Investigators will also aim to characterise the relationship between microcalcification progressing to calcification and the uptake of [18F]NaF. This will be assessed using baseline and follow-up [18F]NaF PET-CT SUVs and their correlation with calcified regions on CT angiography.

Other outcomes

  1. Major adverse cardiovascular events (MACE) and major adverse limb events (MALE)

    Time frame: From baseline imaging to completion imaging at 1 year

    Exploratory endpoints will include major adverse cardiovascular events (acute myocardial infarction, stroke or cardiovascular death) and major adverse limb events (revascularisation or lower limb amputation) as well as death from any cause.

Study contacts

Contact information is provided by the study sponsor or research team.

Allison c Winarski, MBChB, MRCS(Ed)

CONTACT

[email protected]

+447495905258

Rachael O Forsythe, MBChB, PhD, FRCS (Vascular)

CONTACT

[email protected]

+44 01312423585

Sponsors and collaborators

Lead sponsor

University of Edinburgh

Other

Collaborators

  • NHS Lothian

Registry information

Acronym: SISYPHUS

Important dates

Study start
2025
Primary completion
2028
Study completion
2029
First posted
Mar 16, 2026
Registry last updated
Mar 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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