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Coronary Anatomy Study and Times Since the Onset of Acute Myocardial Infarction Symptoms in Women Until the Opening of the Artery (TAPAC Study)

Coronary Anatomy Study and Times Since the Onset of Acute MyocardiaI Infarction Symptoms in Women Until the Opening of the Artery (TAPAC Study)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03152240
Acronym
TAPAC
Enrollment
800
Registered
2017-05-12
Start date
2017-11-01
Completion date
2019-02-26
Last updated
2019-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Infarction

Keywords

Acute Coronary Syndrome, Primary Angioplasty, Gender

Brief summary

TAPAC study is an an investigator-driven, observational, prospective,cohort aimed at evaluating differences between men and women in patients undergoing primary angioplasty : hospital medical care, successful markers myocardial reperfusion and the anatomical substrate by describing the underlying coronary anatomy will be compared.

Detailed description

TAPAC study is an an investigator-driven, observational, prospective,cohort aimed at evaluating differences between men and women in patients undergoing primary angioplasty : hospital medical care, successful markers myocardial reperfusion and the anatomical substrate by describing the underlying coronary anatomy will be compared.

Interventions

OTHERNon intervention

Non intervention

Sponsors

Hospital Universitari Vall d'Hebron Research Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients with: * Aged 18 years or over. * AMI (Acute Mycardial Infarction ) with ST segment elevation and indication of primary angioplasty in whom at least one diagnostic procedure with coronary angiography is performed.

Exclusion criteria

Patients with: * Life expectancy of less than one year. * Previous AMI. * Previous coronary revascularization.

Design outcomes

Primary

MeasureTime frameDescription
Underlying coronary anatomy assessment24 hoursFinal TIMI Thrombus grade
Time from onset of chest pain to arrival Cath Lab24 hoursTime from onset of chest pain to arrival Cath Lab
Time from onset of chest pain to artery opening24 hoursTime from onset of chest pain to artery opening
Door-to-balloon time in patients90 minutesDoor-to-balloon time in patients
Door-to-needle time in patients90 minutesDoor-to-balloon time in patients
Time from onset of chest pain to first medical care24 hoursTime from onset of chest pain to first medical care
Markers successful myocardial reperfusion by angiographyFirst 90 min after reperfusion.ST segment resolution 90 minutes post-PCI (Percutaneous Coronary Intervention)

Secondary

MeasureTime frameDescription
Major adverse cardiac events (MACE)Hospital discharge and expected average of 1 week, one year follow-upMACE rate during hospitalization, defined as death, non-fatal myocardial rupture, or appearance or worsening of heart failure during the hospitalization period and after 1 year of follow-up

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026