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OpenTrials
Completed

NCT Number: NCT01018706

Goodness of Clinical History During Stemi PCI

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Interventional cardiology divisione , Umberto I Hospital

Frosinone, Italy

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Adequacy of medical history collection at the moment of primary pci and 4 days after the index procedure

    Time frame: Adequacy of medical history collection at the moment of primary pci and 4 days after the index procedure

Sponsors and collaborators

Lead sponsor

Umberto I Hospital, Frosinone Italy

Other

Registry information

Official study title

Goodness of Clinical History During Stemi PCI (GHOST)

Acronym: GHOST

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Nov 25, 2009
Registry last updated
Dec 17, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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