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Effect of Thrombus Aspiration in Patients With Myocardial Infarction Presenting Late After Symptom Onset

U

University of Leipzig

Status and phase

Completed
Phase 4

Conditions

Myocardial Infarction

Treatments

Device: manual thrombus aspiration (Export catheter, Medtronic Inc. Minneapolis, Minnesota, USA)

Study type

Interventional

Funder types

Other

Identifiers

NCT01379248
STEMI-Late-Presenter

Details and patient eligibility

About

The purpose of this study is to examine the benefit of thrombus aspiration in patients with ST-elevation myocardial infarction presenting late after symptom onset.

Enrollment

152 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ST-elevation myocardial infarction >12 and <48 hours after symptom onset
  • age 18 to 90 years
  • informed consent

Exclusion criteria

  • prior fibrinolysis
  • severe comorbidities with limited life expectancy
  • pregnancy
  • patient unable to give informed consent
  • participation in another trial
  • contraindications for heparin, aspirin or thienopyridines
  • contraindications for cardiac magnetic resonance examination

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

152 participants in 2 patient groups

thrombus aspiration
Experimental group
Description:
Manual thrombus aspiration with dedicated catheter (Export, Medtronic Inc. Minneapolis, Minnesota, USA)
Treatment:
Device: manual thrombus aspiration (Export catheter, Medtronic Inc. Minneapolis, Minnesota, USA)
no thrombus aspiration
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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