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Systemic SclerosisEVOLVE-SScNCT07717060

Extracellular Vesicle Dynamics Predicting Vascular Complications and Treatment Response in Systemic Sclerosis

A study testing Blood sampling, nailfold capillaroscopy in people with Systemic Sclerosis and Pulmonary Arterial Hypertension, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

Systemic sclerosis is a multisystem autoimmune disease characterized by vascular dysfunction, immune dysregulation, and progressive tissue fibrosis. Cardiopulmonary complications and peripheral vascular involvement are the principal causes of disability and mortality. Read more about this study

Who is it for?
Ages 45 to 75 yearsHealthy volunteers can take part
What is being tested?
Blood sampling, nailfold capillaroscopy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
No sites listed yet
Study dates
1 Sep 2026to 1 Sep 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 45 to 75 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Male and female patients aged 45-75 years Diagnosis of systemic sclerosis according to the 2013 ACR/EULAR classification criteria High risk of pulmonary arterial hypertension based on the DETECT algorithm Stable treatment with vasoactive, vasodilator, and immunosuppressive therapies for at least 3 months prior to blood sampling

Who cannot join

  • Previous diagnosis of pulmonary arterial hypertension confirmed by right heart catheterization Interstitial lung involvement affecting more than 10% of the lung parenchyma Left-sided heart failure (NYHA class 3-4) Evidence of chronic thromboembolic pulmonary disease on contrast-enhanced CT scan Major contraindications to right heart catheterization or coronary angiography Inability to provide informed consent

About this study

Official title: Extracellular Vesicle Dynamics Across the Circulatory System as Predictors of Major Vascular Complications and Therapeutic Response in Systemic Sclerosis Patients

Systemic sclerosis is a multisystem autoimmune disease characterized by vascular dysfunction, immune dysregulation, and progressive tissue fibrosis. Cardiopulmonary complications and peripheral vascular involvement are the principal causes of disability and mortality.

Extracellular vesicles (EVs) have emerged as key mediators of paracrine intercellular communication. Preclinical studies further suggest that EVs mediate long-range inter-organ communication through the circulation. However, the inability to directly track EV trafficking in vivo in humans has limited the understanding of their contribution to systemic inter-organ communication.

Read more

The investigators propose that systemic sclerosis provides a unique human model for investigating circulating EV-mediated inter-organ communication in a multisystem disease. The central hypothesis is that arteriovenous differences in the molecular and cellular characteristics of circulating EVs reflect their dynamic exchange between individual organs and the bloodstream, and that these differences are associated with disease severity. Comparison of EVs across the circulation, rather than relying exclusively on peripheral blood samples, enables a more direct assessment of organ-specific EV release and uptake.

Characterizing EV dynamics along the circulatory pathway has the potential to identify novel biomarkers and therapeutic targets for systemic sclerosis while providing fundamental insights into EV-mediated inter-organ communication in humans.

Read the detailed description

Systemic sclerosis (SSc) is a multi-organ disease characterized by vascular, immune, and fibrotic changes. Vascular complications significantly contribute to mortality, disability, and healthcare costs in patients with SSc. These include digital ulcers (DUs) and associated conditions such as gangrene and osteomyelitis, as well as pulmonary arterial hypertension (PAH), all of which continue to have poor outcomes despite treatment advances. Notably, severe vascular disease increases the risk of cardiac and peripheral atherosclerosis, even in the absence of symptoms or overt risk factors. Timely management improves outcomes, but screening and prognostic stratification tools for SSc remain limited. Evidence supporting personalized treatment selection among currently available therapies is lacking.

Extracellular vesicles (EVs) are subcellular particles that facilitate the transfer of proteins, nucleic acids, and lipids between cells. They have been explored as biomarkers, therapeutic targets, and drug carriers across a wide range of diseases.

The investigators hypothesize that EVs play a direct and distinct role in the pathophysiology of multiorgan complications in SSc, particularly PAH and DUs. This hypothesis is supported by preclinical evidence demonstrating the involvement of EVs in endothelial dysfunction, intimal proliferation, immune dysregulation, and fibrosis, which are key processes in SSc pathogenesis. In mouse models, intravenously administered EVs are primarily taken up by the lungs, and PAH can be induced in healthy mice by injecting EVs isolated from pulmonary hypertensive animals. In humans, circulating EVs in the peripheral blood of patients with PAH are more abundant and exhibit distinct proteomic and transcriptomic profiles compared with those of healthy controls. Preliminary evidence further suggests that EV profiles in the venous blood of patients with SSc may correlate with disease severity and activity, although data specifically addressing vascular complications remain limited.

EVs exert biological effects through their protein, nucleic acid, and lipid cargo, as well as their ability to reach and interact with target cells. Recent studies in transgenic zebrafish have demonstrated that endogenous EVs can extravasate to distant target tissues in vivo. However, direct tracking of EVs in humans remains technically unfeasible with current methods. As a surrogate for in vivo tracking, the investigators propose characterizing circulating EVs at specific vascular locations accessible through acral vessels and during clinically indicated procedures such as right heart catheterization (RHC) and coronary angiography. These procedures, recommended for the assessment of PAH in patients with SSc, are consistent with international guidelines and pose no additional risk, making SSc an ideal model for investigating EV dynamics in humans.

This study aims to map EV characteristics across the circulatory system by evaluating changes at key anatomical sites. Sampling locations include the pulmonary artery and ascending aorta, reflecting pulmonary circulation and cardiac EV exchange, and the peripheral radial artery and cephalic vein, representing EV exchange within the acral circulation. EV profiles at these locations are expected to differ as a result of intravasation, extravasation, and collateral blood flow. Current approaches, which rely exclusively on peripheral venous sampling, lack this regional specificity and capture only the aggregate EV output.

The investigators further propose a comprehensive structural and functional evaluation of the cardiopulmonary and peripheral vascular systems to address the complex and heterogeneous nature of SSc complications. Pulmonary hypertension (PH) may arise from pulmonary vascular disease, including PAH or, less commonly, pulmonary veno-occlusive disease (group 1 PH); SSc-associated cardiac disease, including myocarditis, microvascular dysfunction, or accelerated coronary artery disease (group 2 PH); interstitial lung disease (group 3 PH); or, less frequently, chronic thromboembolic disease (group 4 PH). Similarly, DUs may result from microcirculatory failure or accelerated peripheral atherosclerotic disease. Defining the contribution of these overlapping mechanisms in individual patients is essential for interpreting and generalizing EV-related findings.

The unique characteristics of SSc among human diseases may provide broader insights into EV dynamics within the human circulatory system, potentially informing future research on other vascular and multiorgan diseases.

Being tested
Blood sampling, nailfold capillaroscopy
Medical subject headings
Scleroderma, Systemic, Pulmonary Arterial Hypertension, digital ulcers

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Blood sampling, nailfold capillaroscopyDiagnostic test

    Blood collection during right heart catheterization

Study groups in NCT07717060
Study groupRoleWhat they receive
Diagnosis of systemic sclerosis according to the 2013 ACR/EULAR classification criteria.Experimental* Male and female patients aged 45-75 years. * Diagnosis of systemic sclerosis according to the 2013 ACR/EULAR classification criteria. * High risk of pulmonary arterial hypertension based on the DETECT algorithm. * Stable treatment with vasoactive, vasodilator, and immunosuppressive therapies for at least 3 months prior to blood sampling.
Receives: Diagnostic Test: Blood sampling, nailfold capillaroscopy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Transcardiopulmonary extracellular vesicle gradient

    Arteriovenous differences between the pulmonary artery and the ascending aorta in extracellular vesicle characteristics, including particle concentration, size distribution, protein expression profile, and RNA expression profile.

    Treatment failure in patients with pulmonary arterial hypertension at 24 weeks, defined as the occurrence of at least one of the following events: an improvement of less than 30 meters in the 6-minute walk distance (6MWD); a reduction in NT-proBNP of less than 30% in patients with baseline levels >300 pg/mL; worsening of World Health Organization (WHO) functional class; or death due to complications of pulmonary arterial hypertension.

    Treatment failure in patients with recurrent digital ulcers, defined as the development of new digital ulcers or gangrene at sites previously affected by digital ulcers.

    Measured: Periprocedural (during right heart catheterization).

  2. Peripheral extracellular vesicle gradient

    Arteriovenous differences between the cephalic vein and the radial artery in extracellular vesicle characteristics, including particle concentration, size distribution, protein expression profile, and RNA expression profile.

    Measured: Periprocedural.

Secondary outcomes (2)
  1. Treatment failure in participants with pulmonary arterial hypertension.

    Treatment failure, defined as the occurrence of at least one of the following: improvement in 6-minute walk distance of less than 30 meters; reduction in NT-proBNP of less than 30% in participants with baseline NT-proBNP >300 pg/mL; worsening of World Health Organization functional class; or death related to pulmonary arterial hypertension.

    Measured: 24 weeks.

  2. Treatment failure in participants with recurrent digital ulcers.

    Development of new digital ulcers or gangrene at sites previously affected by digital ulcers.

    Measured: 24 weeks.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Jul 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion1 Sep 2027 (estimated)
  4. Study completion1 Sep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07717060
Sponsor's protocol ID
27513
Acronym
EVOLVE-SSc
Status last verified
Jul 2026
First submitted
9 Jul 2026
Last updated
21 Jul 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: All data will be shared, excluding the patient's first and last name.

Questions about this trial

What is this clinical trial studying?

A study testing Blood sampling, nailfold capillaroscopy in people with Systemic Sclerosis and Pulmonary Arterial Hypertension, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 21 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Transcardiopulmonary extracellular vesicle gradient (time frame: Periprocedural (during right heart catheterization).). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jul 2026.

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