Coronary PatientsCOMPARNCT00699959

National Survey on Coronary Patients and Heart Failure Performed in 2 Patient Groups

An observational study of Coronary Patients and Heart Failure, run by AstraZeneca at 324 sites in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Trial summary

The purpose of this observational study is to compare frequency of attainment control goals through the more represented cardiovascular factor risk, dyslipidemia, among coronary patients with or without heart failure in cardiology consulting. Read more about this study

Who is it for?: Ages 18 years and older
Conditions the study is for: Coronary Patients, Heart Failure
How many people: 1,650 participants
Where: 324 sitesFrance
Study dates: Jun 2008to Jan 2009
Phase: Observational
Are there results?: None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

Ages 18 years and older
All sexes
No healthy volunteers
Adult, Older adult

Study population: First two consecutive Coronary patients with or without heart failure

Who may be able to join

patient with coronary disease diagnosed since at least 1 year
Echocardiography done less than 1 year ago
patient with or without documented heart failure

Who cannot join

None

Trial locations and contacts

324 sites in 1 country.

City, postcode or hospital

300 sites in 1 country

France300 sites

Research Site
Abbeville
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Aix-en-Provence
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Aix-les-Bains
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Ajaccio
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Albi
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Alençon
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Alès
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Amboise
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Amiens
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Andrézieux-Bouthéon
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Angers
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Angoulême
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Annecy
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Annemasse
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Antibes
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Antony
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Arès
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Argentan
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Arles
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Armentières
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Arnouville
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Arras
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Asnières-sur-Seine
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Auch
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Auchel
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Audincourt
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Aulnay-sous-Bois
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Avallon
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Bagnères-de-Bigorre
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Bagnolet
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Bagnols-sur-Cèze
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Bailleul
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Balma
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Bar-le-Duc
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Bastia
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Bayonne
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Beaumont-de-Lomagne
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Beausoleil
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Beauvais
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Belfort
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Belley
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Bergerac
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Besançon
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Béthune
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Béziers
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Biarritz
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Blois
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Bois-Colombes
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Bois-Guillaume
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Bonneuil-sur-Marne
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Bordeaux
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Boulogne-Billancourt
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Bourg-en-Bresse
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Bourges
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Brest
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Briey
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Brive-la-Gaillarde
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Bron
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Caen
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Cagnes-sur-Mer
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Cahors
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Cannes
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Cannes La Bocca
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Carcassonne
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Carpentras
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Castelnaudary
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Castres
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Cavaillon
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Cenon
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Cergy
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Cesson-Sévigné
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Challans
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Chalon-sur-Saône
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Chambéry
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Chamonix
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Champigny-sur-Marne
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Chantilly
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Charleville-Mézières
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Chartres
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Château-d'Olonne
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Châteaubernard
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Châteauroux
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Châtillon
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Châtillon-sur-Seine
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Chaville
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Cherbourg Octeville
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Choisy-le-Roi
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Cholet
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Clamart
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Clermont-Ferrand
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Commercy
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Condé-sur-l'Escaut
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Conflans STE Honorine
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Corbeil-Essonnes
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Cornebarrieu
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Cournon-d'Auvergne
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Coutances
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Creil
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Croix
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Dax
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Décines-Charpieu
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Denain
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Dieulefit
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Dijon
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Divion
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Dol-de-Bretagne
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Douai
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Draguignan
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Drancy
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Dunkirk
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Épernay
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Épinal
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Erstein
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Étampes
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Évecquemont
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Évian-les-Bains
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Floirac
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Frontignan
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Genas
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Gennevilliers
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Grande-Synthe
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Grenoble
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Grésy-sur-Aix
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Guebwiller
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Guéret
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Guyancourt
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Haguenau
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Harfleur
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Hayange
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Hazebrouck
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Hénin-Beaumont
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Hesdin
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Hyères
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Issy-les-Moulineaux
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Juan-les-Pins
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L'Haÿ-les-Roses
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L'Île-Rousse
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La Bassée
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La Chaussée-Saint-Victor
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La Ciotat
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La Courneuve
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La Flèche
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La Madeleine
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La Rochelle
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La Seyne-sur-Mer
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La Verpillière
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Lagny-sur-Marne
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Lamballe
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Lanester
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Langon
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Lannemezan
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Le Bourget
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Le Chesnay
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Le Havre
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Le Kremlin-Bicêtre
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Le Mans
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Le Perreux-sur-Marne
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Le Plessis-Trévise
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Le Port-Marly
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Le Raincy
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Les Clayes-sous-Bois
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Les Sables-d'Olonne
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Les Ulis
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Levallois-Perret
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Lille
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Limoges
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Limoux
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Lisieux
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Lomme
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Longeville-lès-Metz
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Lons-le-Saunier
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Lorient
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Lunel
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Lyon
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Mâcon
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Malo-les-Bains
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Marcq-en-Barœul
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Marcy-l'Étoile
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Maromme
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Marseille
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Maubeuge
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Maurepas
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Mayenne
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Meaux
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Mende
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Menton
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Metz
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Millau
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Milly-la-Forêt
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Miramas
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Monaco
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Mont-de-Marsan
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Montargis
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Montauban
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Montélimar
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Montesson
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Montfermeil
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Montigny-lès-Metz
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Montpellier
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Montreuil
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Morlaix
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Mulhouse
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Muret
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Nancy
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Nanterre
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Nantes
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Neufchâteau
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Neuville-sur-Saône
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Nice
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Nîmes
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Niort
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Noisy-le-Grand
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Olivet
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Ollioules
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Orléans
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Ornans
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Orsay
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Oullins
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Ozoir-la-Ferrière
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Palaiseau
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Pantin
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Paray-le-Monial
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Paris
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Pau
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Périgueux
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Perpignan
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Pessac
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Pithiviers
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Plaisance-du-Touch
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Plan-de-Cuques
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Ploërmel
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Poitiers
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Pont-à-Mousson
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Pontarlier
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Pontault-Combault
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Pontoise
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Prévessin-Moëns
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Quimper
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Quincy-sous-Sénart
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Reims
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Rennes
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Revel
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Ris-Orangis
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Rodez
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Rognac
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Romans-sur-Isère
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Rosny-sous-Bois
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Roubaix
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Royat
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Rueil-Malmaison
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Sablé-sur-Sarthe
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Saint-Avertin
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Saint-Avold
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Saint-Brieuc
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Saint-Chamond
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Saint-Doulchard
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Saint-Etienne
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Saint-Fargeau-Ponthierry
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Saint-Fons
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Saint-Gély-du-Fesc
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Saint-Genis-Laval
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Saint-Germain-en-Laye
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Saint-Julien-en-Genevois
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Saint-Lô
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Saint-Louis
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Saint-Martin-Boulogne
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Saint-Maur-des-Fossés
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Saint-Nazaire
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Saint-Orens-de-Gameville
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Saint-Ouen
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Saint-Pierre-des-Corps
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Saint-Pol-de-Léon
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Saint-Priest
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Saint-Quentin
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Saint-Raphaël
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Sanary-sur-Mer
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Sarcelles
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Sarrebourg
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Sarreguemines
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Sceaux
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Schiltigheim
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Sélestat
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Somain
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Sorgues
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St.-Jean
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Strasbourg
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Suresnes
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Tarbes
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Taverny
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Tergnier
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Ternay
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Thann
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Thiais
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Thionville
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Toulon
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Toulouse
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Tournefeuille
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Tours
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Trappes
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Troyes

Other trials in France

About this study

Official title: Comparison and Description of Coronary Patients Management With or Without Heart Failure in Cardiology Consulting

Conditions: Coronary Patients, Heart Failure
Keywords: Coronary patients, heart failure, dyslipidemia
Medical subject headings: Heart Failure, Dyslipidemias

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT00699959
Study group	Role	What they receive
1		patients with heart failure
2		patients without heart failure

What is being measured

The primary outcome is the main question the study is designed to answer.

Frequency of attainment control goals through the more represented cardiovascular factor risk, dyslipidemia, among coronary patients with or without heart failure in cardiology consulting.
Measured: Once

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

Jun 2008Jan 2009

First posted18 Jun 2008 (estimated)
Study startJun 2008
Study completionJan 2009

Resources

Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
Other trials for Coronary PatientsStudies of the same condition, open and under way.
More trials run by AstraZenecaThe sponsor's other registered studies.
What the trial phases meanHow a treatment moves from first tests in people to approval.

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design

Study type: Observational
Observational model: Cohort
Time perspective: Cross-sectional
Enrolment: 1,650 participants (actual)

IDs, dates and publications

ClinicalTrials.gov ID: NCT00699959
Sponsor's protocol ID: NIS-CFR-DUM-2007/8
Acronym: COMPAR
Status last verified: Aug 2009
First submitted: 16 Jun 2008
Last updated: 6 Aug 2009
Results posted: No
Data monitoring committee: No

Want to know more?

The sponsor has not listed a contact. The official record may have more details.

Talk to your doctor first and take this page with you. Only the study team can confirm whether you can join.

Questions to ask the study team

What is the study trying to find out?
What would I need to do, and how often would I visit?
Could I receive a placebo instead of the treatment?
What are the possible risks and benefits for me?
Will it cost me anything? Are travel or time paid for?
Can I keep seeing my own doctor during the study?
What happens when the study ends?

See locations

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Effect of Stress Ball Use During Femoral Arterial Sheath Removal After Coronary Angiography
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AI-powered ECG Analysis Using Willem™ Software in High-risk Cardiac Patients (WILLEM)
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RecruitingPhase 4
The Effects of Ferric Derisomaltose in Patients With Acute Heart Failure and Iron Deficiency on Exercise Capacity and Quality of Life(COREVIVE-HFrEF)
Heart Failure With Reduced Ejection Fraction, Iron Deficiency
Not yet recruitingPhase 2
A Study of Bimagrumab in Participants With HFpEF
Heart Failure, Diastolic, Diastolic Heart Failure
Not yet recruitingObservational study
Systematic Intraoperative Cell Salvage in On-Pump Cardiac Surgery Within a Mature Patient Blood Management Programme
Cardiac Surgical Procedures, Blood Transfusion

All Coronary Patients trials

Study at a glance

From the registry record, last updated by the sponsor on 6 Aug 2009. Recruitment status is as the sponsor reported it: confirm with the study team.

Official title: Comparison and Description of Coronary Patients Management With or Without Heart Failure in Cardiology Consulting
ClinicalTrials.gov ID: NCT00699959
Acronym / sponsor ID: COMPAR / NIS-CFR-DUM-2007/8
Conditions: Coronary Patients, Heart Failure
Keywords: Coronary patients, heart failure, dyslipidemia
Study type: Observational
Recruitment status: Completed
Enrolment: 1,650 participants (actual)
Lead sponsor: AstraZenecaIndustry (pharma, biotech, devices)
Study start: Jun 2008
Study completion: Jan 2009 (actual)
First posted: 18 Jun 2008 (estimated)
Results: Not posted in the source record

Clinical summary

The research question as the sponsor registered it. This describes what the study plans to test, not what it found.

Study design

Observational model: Cohort
Time perspective: Cross-sectional
Number of arms: 2

Arm	Type	Receives
1	–	–patients with heart failure
2	–	–patients without heart failure

Who may qualify

Ages: 18 years and older
Sex: All
Healthy volunteers: Not accepted
Age groups: Adult, Older adult
Study population: First two consecutive Coronary patients with or without heart failure

Key inclusion criteria (3 listed)

patient with coronary disease diagnosed since at least 1 year
Echocardiography done less than 1 year ago
patient with or without documented heart failure

Key exclusion criteria (1 listed)

None

Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.

Primary outcome

Frequency of attainment control goals through the more represented cardiovascular factor risk, dyslipidemia, among coronary patients with or without heart failure in cardiology consulting.
Time frame: Once

Results and safety

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

Research links

Official record on ClinicalTrials.govLast updated by the sponsor 6 Aug 2009.

Related trials for Coronary Patients

Not yet recruiting
Effect of Stress Ball Use During Femoral Arterial Sheath Removal After Coronary Angiography
Femoral Arterial Sheath Removal, Stress Ball
RecruitingObservational study
AI-powered ECG Analysis Using Willem™ Software in High-risk Cardiac Patients (WILLEM)
Cardiomyopathies, Cardiac Arrest
RecruitingPhase 4
The Effects of Ferric Derisomaltose in Patients With Acute Heart Failure and Iron Deficiency on Exercise Capacity and Quality of Life(COREVIVE-HFrEF)
Heart Failure With Reduced Ejection Fraction, Iron Deficiency
Not yet recruitingPhase 2
A Study of Bimagrumab in Participants With HFpEF
Heart Failure, Diastolic, Diastolic Heart Failure
Not yet recruitingObservational study
Systematic Intraoperative Cell Salvage in On-Pump Cardiac Surgery Within a Mature Patient Blood Management Programme
Cardiac Surgical Procedures, Blood Transfusion

Referral and contact

AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.

Alain Castaigne study director

AstraZeneca

324 sites in 1 country: see every site and its status.

Questions about this trial

What is this clinical trial studying?

An observational study of Coronary Patients and Heart Failure, run by AstraZeneca at 324 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Aug 2009. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 324 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Frequency of attainment control goals through the more represented cardiovascular factor risk, dyslipidemia, among coronary patients with or without heart failure in cardiology consulting. (time frame: Once). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00699959.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Aug 2009.