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Heart attack stents face off: which heals better?

NCT ID NCT02890589

Knowledge-focused Sponsor: University Hospital, Toulouse Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how well two types of stents (small mesh tubes) placed in heart arteries after a heart attack become covered by the body's own cells. 22 people who had a heart attack were randomly assigned to get either a SYNERGY stent or a bioresorbable scaffold. Doctors used a special camera inside the artery at 3 months to count how many parts of the stent were still uncovered. The goal was to see which device helps the artery heal faster.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

22 people

The number who actually took part.

Started

Jul 2016

Finished

Feb 2018

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 85 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Acute coronary syndrome with ST-elevation, * One culprit lesion eligible for percutaneous coronary intervention (PCI) with stent implantation, * Reference vessel measuring 2.5 mm to 3.75 mm per visual estimation, without extreme vessel tortuosity, * thrombolysis in myocardial infarction (TIMI) 3 flow before stent deployment in the target vessel, * Patient with at least 1 lesion eligible for planned PCI next to the culprit lesion, * Patient affiliated to the French national health care system, * Patient agreed to participate after full information on the study (signature of an informed consent). Exclusion Criteria: * Acute coronary syndrome with ST-elevation, * One culprit lesion eligible for percutaneous coronary intervention (PCI) with stent implantation, * Reference vessel measuring 2.5 mm to 3.75 mm per visual estimation, without extreme vessel tortuosity, * TIMI 3 flow before stent deployment in the target vessel, * Patient with at least 1 lesion eligible for planned PCI next to the culprit lesion, * Patient affiliated to the French national health care system, * Patient agreed to participate after full information on the study (signature of an informed consent).

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Conditions

The condition(s) this trial relates to.

acute coronary syndrome acute myocardial infarction

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Acute coronary syndrome

Contacts and locations

Locations

  • Didier CARRIE

    Toulouse, Toulouse, 31500, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.