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Heart stent showdown: which technique wins?

NCT ID NCT00292305

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested two ways to place stents in heart arteries that have a branch (bifurcation). 425 patients with chest pain were randomly assigned to either the 'crush' or 'culotte' technique. Researchers tracked heart-related deaths, heart attacks, stent clots, and the need for repeat procedures to see which method works better.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
drug-eluting stent
What this could lead to
If successful, this could help doctors choose the better stenting technique for patients with complex heart artery blockages, potentially reducing heart attacks and repeat procedures.
What could go wrong
This is a completed Phase 4 trial, so results are already known. The comparison may show no clear winner, or one technique may have higher risks like stent thrombosis. Findings may not apply to all patients.

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

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

425 people

The number who actually took part.

Start date

Sep 2005

Finished

Dec 2012

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * Stable or unstable AP. * Bifurcation lesion of "LAD/diagonal", "Cx/obtuse marginal", "RCA-PDA/posterolateral branch" or "LM/Cx/LAD". * Diameter of main vessel by visual estimate \> 3.0 mm. * Diameter of side branch by visual estimate \> 2.5 mm. * Signed informed consent Exclusion Criteria: * ST-elevation AMI within 24 hours. * Expected survival \< 1 year. * S-creatinine \> 200 Umol/l. * Allergy to aspirin, clopidogrel or ticlopidine. * Allergy to sirolimus. * Left main bifurcation in a non-right dominant system.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Skejby Hospital, University of Aarhus

    Aarhus, 8200, Denmark

More trials for these conditions

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