France PCI Registry : National Observatory of Interventional Cardiology

Rigorous clinical practice assessment is a key factor to improve patient's care and prognosis in interventional cardiology (IC). A multicentric IC observational study (CRAC), fully integrated to usual coronary activity report software, started in Centre Val de Loire (CVL) region in 2014.

CRAC observatory was conduced on five IC CathLab of CVL region. Quality of collected data is regularly evaluated and allowed building an exhaustive, and reliable database. This solution could easily be developed in other French regions.

Study Overview

• Status: Recruiting
• Conditions: STEMI; Interventional; Angioplasty; Cardiology; Database; Coronary

• Study Type: Observational
• Enrollment (Anticipated): 40000

Contacts and Locations

• Study Contact: Name: Gregoire Range, MD; Email: registrecrac@ch-chartres.fr

Study Locations

• France
  • Aurillac, France, 15002
    • Recruiting
    • Centre Hospitalier Henri Mondor d'Aurillac
    • Contact: Louis Viallard, MD
    • Principal Investigator: Louis Viallard, MD
  • Bourges, France, 18020
    • Recruiting
    • Centre Hospitalier Jacques Coeur de Bourges
    • Contact: Pierre Marcollet, MD
    • Principal Investigator: Pierre Marcollet, MD
  • Caen, France, 14033
    • Recruiting
    • CHU Caen - Hôpital Côte de Nacre
    • Contact: Farzin Beygui, MD
    • Principal Investigator: Farzin Beygui, MD
  • Caen, France, 14050
    • Not yet recruiting
    • Hôpital Privé Saint-Martin Caen
    • Contact: Jean François Morelle, MD
    • Principal Investigator: Jean François Morelle, MD
  • Chambray-lès-Tours, France, 37170
    • Recruiting
    • CHRU Hôpitaux de Tours - Trousseau
    • Contact: Denis Angoulvant, MD
  • Clermont-Ferrand, France, 63003
    • Recruiting
    • CHU Gabriel-Montpied de Clermont-Ferrand
    • Contact: Pascal Motreff, MD
    • Principal Investigator: Pascal Motreff, MD
  • Le Havre, France, 76620
    • Recruiting
    • Hôpital Privé de l'Estuaire
    • Contact: Pierre François Lesault, MD
    • Principal Investigator: Pierre François Lesault, MD
  • Montivilliers, France, 76290
    • Recruiting
    • Groupe Hospitalier du Havre - Hôpital Jacques Monod
    • Contact: Philippe Bonnet, MD
    • Principal Investigator: Philippe Bonnet, MD
  • Orléans, France, 45100
    • Recruiting
    • CHR Orléans - Hôpital de la Source
    • Contact: Wael Yafi, MD
    • Principal Investigator: Wael Yafi, MD
  • Rouen, France, 76031
    • Recruiting
    • CHU de Rouen - Hôpital Charles-Nicolle
    • Contact: Eric Durand, MD
  • Rouen, France, 76044
    • Recruiting
    • Clinique Saint-Hilaire - Rouen
    • Contact: René Koning, MD
    • Principal Investigator: René Koning, MD
  • Saran, France, 45770
    • Recruiting
    • Pôle Santé Oréliance - Clinique de la Reine Blanche
    • Contact: Philippe Dequenne, MD
    • Principal Investigator: Philippe Dequenne, MD
  • Tours, France, 37042
    • Recruiting
    • Clinique Saint-Gatien
    • Contact: Stephan Chassaing, MD
    • Principal Investigator: Stephan Chassaing, MD
  • Évreux, France, 27025
    • Not yet recruiting
    • Clinique Bergouignan
    • Contact: Gérard Dutheil, MD
    • Principal Investigator: Gérard Dutheil, MD
  • Eure Et Loire
    • Le Coudray, Eure Et Loire, France, 28630
      • Recruiting
      • Research Cardiology Unit / Les hopitaux de Chartres
      • Contact: Sandra Gautier
      • Contact: Christophe Laure
      • Principal Investigator: Grégoire Rangé, MD

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

patients aged over 18 undergoing coronary angiogram or angioplasty

Description

Inclusion Criteria:

• Age =>18 years at enrollment
• Patient who have had a coronary angiogram or angioplasty

Exclusion Criteria:

• Patient who didn't want to participated

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Census of interventional cardiology activity	Census, follow-up and monitoring of patients during 1 year, after a coronary angioplasty	1 year

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Optimization of STEMI patient care time	Manage STEMI < H24 patients, record and monitor time intervals from first pain to first medical contact in order to achieve and maintain the quality of care	Less than 24 hours

Collaborators and Investigators

• Sponsor: Club Régional des Angioplasticiens de la région Centre
• Collaborators: Direction Générale de l'Offre de Soins; Agence Régional de Santé du Centre; France PCI Association

Study record dates

Study Major Dates

• Study Start: January 1, 2014
• Primary Completion (Anticipated): January 1, 2030
• Study Completion (Anticipated): December 1, 2030

Study Registration Dates

• First Submitted: May 18, 2016
• First Submitted That Met QC Criteria: May 18, 2016
• First Posted (Estimate): May 20, 2016

Study Record Updates

• Last Update Posted (Actual): April 7, 2022
• Last Update Submitted That Met QC Criteria: March 29, 2022
• Last Verified: March 1, 2022

More Information

Terms related to this study

• Other Study ID Numbers: France PCI