GensiniMI: Gensini Score and STEMI Patients Undergoing Primary PCI
Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05679843
Collaborator
(none)
1,200
3.9
Study Details
Study Description
Brief Summary
Gensini score (GS) provides valuable information on severity and prognosis of coronary artery disease (CAD). We aim to evaluate the relationship between the severity of CAD determined by the GS and short and long term of ST-elevation myocardial infarction (STEMI) patients undergoing primary percutaneous coronary intervention.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational [Patient Registry]
Anticipated Enrollment
:
1200 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Characteristics and Prognosis of STEMI Patients Undergoing Primary PCI With Low
Anticipated Study Start Date
:
Jan 1, 2023
Anticipated Primary Completion Date
:
Mar 30, 2023
Anticipated Study Completion Date
:
May 1, 2023
Outcome Measures
Primary Outcome Measures
- Composite outcome including all cause death and re myocardial infarction [6 years]
Secondary Outcome Measures
- ST resolution on ECG after primary PCI [1 hour]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
- Patients with STEMI underwent primary PCI within 24 hours after first symptoms
Exclusion Criteria:
Patients with STEMI 24 hours after first symptoms Pregnant patient <18 years old
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Central Hospital, Nancy, France
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Batric POPOVIC,
MD,PhD,
Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT05679843
Other Study ID Numbers:
- CentralGensini
First Posted:
Jan 11, 2023
Last Update Posted:
Jan 11, 2023
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Batric POPOVIC,
MD,PhD,
Central Hospital, Nancy, France
Additional relevant MeSH terms: