Goodness of Clinical History During Stemi PCI

NCT ID: NCT01018706

Last Updated: 2013-12-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

400 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-03-31

Study Completion Date

2012-03-31

Brief Summary

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The purpose of this study is to confirm or confute the hypothesis that in patients treated with primary pci is not always possible to collect an adequate medical history, the investigators created a clinical registry in which the investigators collect current or previous medical history relevant to DES utilization , in two distinct times.

Detailed Description

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GHOST Registry

Use of drug-eluting stent (DES) in STEMI is sometimes limited, by the concern that adequate information, relating to the current or previous medical history, can not be obtained due to the patient's critical condition. A less than adequate medical history would expose patients treated with DES to a particular risk in case that an absolute or relative contraindication to the required long-term double antiplatelet therapy is not fully elucidated before DES implantation.

To confirm or confute the hypothesis that in patients treated with primary pci is not always possible to collect an adequate medical history, we created a clinical registry in which we collect current or previous medical history relevant to DES utilization , in two distinct times:

Time zero in which the medical history collection is taken in the cath-lab during the primary pci

Time one in which the second medical history collection is taken 4 days after the index procedure when the patient clinical conditions no longer impede an adequate medical history collection.

Conditions

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Myocardial Infarction

Keywords

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Primary pci Stent Medical Hystory Antiplatelet therapy Compliance

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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STEMI patients treated with PCI

Four hundred patients with STEMI treated with primary PCI or rescue PCI.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* All consecutive patients presenting with STEMI treated with primary or rescue PCI

Exclusion Criteria

* Patient in cardiogenic shock and all those patients unable to communicate with the doctors at the moment of medical history taking
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Umberto I Hospital, Frosinone Italy

OTHER

Sponsor Role lead

Responsible Party

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Menichelli Maurizio

Director of Cardiology Division

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Interventional cardiology divisione , Umberto I Hospital

Frosinone, Frosinone, Italy

Site Status

Countries

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Italy

Other Identifiers

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GHOST

Identifier Type: -

Identifier Source: org_study_id