AzTrials
AzTrials

Coronary Artery Disease (CAD)DESPORTNCT07477405

Drug-coatEd Balloon Multicentric Registry in Spain and PORTugal

An observational study of Coronary Artery Disease (CAD) and ST-elevation Myocardial Infarction (STEMI), run by Portuguese Association of Interventional Cardiology.

Not yet recruiting

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

Sites and contacts
Official record
Search all trials

Trial summary

Drug-eluting stents (DES) have been the main treatment option for coronary angioplasty (PCI) for many years. The antiproliferative drug in DES has the effect of preventing in-stent restenosis, which is typically a consequence of intimal hyperplasia, a characteristic phenomenon of bare metal stents (BMS). Read more about this study

Who is it for?
Ages 18 years and older
How many people
1,200 participants
Where
No sites listed yet
Study dates
1 Aug 2026to 30 Dec 2029
How long will I take part?
2 Years
Phase
Observational
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 18 years and older
  • All sexes
  • Adult, Older adult

Study population: Patients undergoing percutaneous coronary intervention (PCI) in which a drug-coated balloon (DCB) is used in at least one coronary lesion.

Who may be able to join

  • Patient over the age of 18 years, undergoing PCI with at least one DCB attempted.
  • Patient has provided written informed consent as approved by the Ethics Committee (EC)
  • Patient is willing to undergo all registry procedures and follow-up requirements

Who cannot join

  • Patients with known allergy to antiplatelet drugs or DCB antiproliferative agents
  • Life expectancy less than 12 months
  • Cardiogenic shock
  • Left ventricular ejection fraction < 15%.
  • Any condition, which in the investigator opinion, would preclude safe participation of the patient in the registry.

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

About this study

Drug-eluting stents (DES) have been the main treatment option for coronary angioplasty (PCI) for many years. The antiproliferative drug in DES has the effect of preventing in-stent restenosis, which is typically a consequence of intimal hyperplasia, a characteristic phenomenon of bare metal stents (BMS).

DES have shown to be safe and effective in many clinical and anatomical scenarios. There are, however, several caveats to DES, like restenosis, thrombosis, accelerated atherosclerosis, impossibility of surgical revascularization and disruption of vessel dynamics.

Read more

These phenomena have a very meaningful negative impact on patient outcomes. Drug-coated balloons (DCB) may avoid those limitations of DES and are an appealing alternative in many different scenarios. They have been the mainstay treatment of in-stent restenosis (ISR) and were formally recommended for this setting in internationally, although recent guidelines recommend DES over a DCB for a first DES restenosis. There is, however, solid evidence for their use in the context of any ISR (BMS or DES-related) and both comparing with POBA or DES. The presence of metal from previous stents makes the implantation of more stents even more of a thing to avoid.

High bleeding risk may also be an advantageous setting for DCB, as it may allow for a shorter or less intensive anti-thrombotic treatment with the same or even improved safety endpoints when compared to BMS or DES with standard therapy.

Other than ISR, there are other particularly appealing anatomical settings for DCBs such as bifurcations, small vessels and diffuse disease. In the setting of a bifurcation where only the side branch is to be treated, there is evidence that DCB is a good option and provides significantly less late luminal loss when compared to POBA. In case a stent is used in the main branch, a DCB is also a good option for the side branch.

In small vessels (<3,0mm), in which the stent metal would be more conspicuous relative to the smaller lumen, there is strong evidence pointing to a benefit of DCB when compared to balloon angioplasty (POBA) and results at least as good as full-DES. A similar MACE rate between DCB and DES has been reported, with a benefit for DCB in terms of bleeding. In fact, also in larger vessels, DCB may lead to similarly good outcomes. DCB (alone or in combination with DES) is a good alternative to DES-only in diffuse disease.

Provided that a good lesion preparation is achieved and there is no structural compromise to the vessel, the lack of a metal stent will be of benefit for any type of lesion. It will contribute to late lumen enlargement (LLE), which can happen in 40-56% of lesions treated with DCB7 and is associated with layered plaques by OCT and medial dissection after lesion preparation.

Evidence for DCBs is increasing in different anatomical and clinical contexts, and there are some dedicated recommendations and consensus regarding their use. There is some data regarding real-world clinical performance of DCBs, but there is still the need for large real-world studies with different DCBs, techniques, clinical settings and anatomical contexts with long term follow-up, which is the main driver for this registry.

Keywords
Drug-coated balloons, Percutaneous Coronary Intervention, DEB, PCI
Medical subject headings
Coronary Artery Disease, ST Elevation Myocardial Infarction

What is being measured

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

  1. Target Lesion Failure (TLF)

    Target Lesion Failure (TLF) defined as a composite of:

    1. Cardiac Death
    2. Target vessel Myocardial infarction (MI)
    3. Clinically driven target lesion revascularization (TLR)

    Measured: 2 Years

Secondary outcomes (2)
  1. Efficacy Endpoints

    1. Target lesion revascularization (TLR)
    2. Target vessel revascularization (TVR)

    Measured: 30 days and 2 Years

  2. Safety Endpoints

    1. Major Adverse Cardiovascular Events (MACE) defined as a composite of :
    2. All-cause mortality
    3. MI (target-vessel and non-target-vessel MI)
    4. Clinically driven TLR
    5. All-cause mortality
    6. Cardiovascular mortality
    7. Myocardial infarction
    8. Stroke (ischemic or haemorrhagic)
    9. Acute kidney injury (AKI)
    10. Major bleeding

    Measured: 2 Years

Timeline

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

  1. First posted17 Mar 2026
  2. Study start1 Aug 2026 (estimated)
  3. Primary completion30 Sep 2029 (estimated)
  4. Study completion30 Dec 2029 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,200 participants (estimated)
Target duration
2 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT07477405
Sponsor's protocol ID
DESPORT-1
Acronym
DESPORT
Status last verified
Mar 2026
First submitted
13 Mar 2026
Last updated
17 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Coronary Artery Disease (CAD) and ST-elevation Myocardial Infarction (STEMI), run by Portuguese Association of Interventional Cardiology.

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 3 inclusion and 5 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 17 Mar 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?

Contact David Neves, MD (+351 217 970 685, dcneves25@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Target Lesion Failure (TLF) (time frame: 2 Years). 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 17 Mar 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in