- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01007734
Factors Determining Quality of Life Related to Respiratory Status According to Gender of Chronic Obstructive Pulmonary Disease (COPD) Patients (VITALITE)
July 26, 2010 updated by: AstraZeneca
Factors Determining Quality of Life Related to Respiratory Status According to Gender of COPD Patients Followed by a Pneumologist
The purpose of this study is to evaluate with sufficient precision and according to gender the determining independent factors of quality of life related to respiratory status of patient with moderate to severe COPD.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
449
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Abbeville, France
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Agde, France
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Agen, France
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Aix En Provence, France
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Ajaccio, France
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Albi, France
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Alencon, France
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Ales, France
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Ambilly, France
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Amelie Les Bains Palalda, France
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Amiens, France
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Angers, France
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Angouleme, France
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Annecy, France
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Antibes, France
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Antony Cedex, France
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Armentieres, France
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Auch, France
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Bagneux, France
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Bastia, France
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Bayonne, France
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Beauvais Cedex, France
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Belfort, France
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Berck Cedex, France
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Besancon, France
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Bethune, France
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Beuvry, France
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Beziers, France
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Bois Guillaume, France
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Bonneville, France
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Bordeaux, France
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Bourges, France
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Bourgoin Jallieu, France
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Brest, France
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Briey Cedex, France
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Brive La Gaillarde, France
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Cachan, France
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Caen Cedex 4, France
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Cagnes Sur Mer, France
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Calais Cedex, France
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Cambo Les Bains, France
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Cambrai, France
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Cannes, France
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Castelnau Le Lez Cedex, France
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Cavaillon, France
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Challans, France
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Chalon Sur Saone, France
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Chalons En Champagne Cedex, France
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Chamalieres, France
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Chambery, France
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Charleville Mezieres, France
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Cherbourg Octeville, France
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Cholet, France
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Clermont Ferrand, France
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Cluses, France
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Cognac, France
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Colmar, France
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Corbeil Essonnes, France
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Corbeil Essonnes Cedex, France
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Courbevoie, France
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Croix, France
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Denain Cedex, France
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Divion, France
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Ecully, France
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Epernay, France
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Facture, France
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Figeac, France
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Fleury Les Aubrais, France
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Foix, France
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Fontenay Le Comte, France
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Frejus, France
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GAP, France
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Givors Cedex, France
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Grande Synthe, France
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Grenoble Cedex 1, France
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Guingamp, France
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Hagondange, France
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Herblay, France
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Hyeres, France
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Istres, France
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Jonzac Cedex, France
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Juan Les Pins, France
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Juvisy Sur Orge Cedex, France
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L Isle D Espagnac, France
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La Ferte Bernard, France
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La Rochelle, France
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La Teste de Buch, France
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Lagny Sur Marne Cedex, France
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Laon, France
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Le Cannet, France
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Le Chesnay, France
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Lege Cap Ferret, France
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Lens Cedex, France
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Libourne, France
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Lievin Cedex, France
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Lille, France
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Limoges, France
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Lodeve, France
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Lorient, France
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Lormont, France
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Lutterbach, France
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Lyon, France
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Maisons Alfort, France
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Maisons Laffitte Cedex, France
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Mandelieu La Napoule, France
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Marignane, France
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Marly Le Roi, France
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Marmande, France
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Marseille, France
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Melun, France
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Mende, France
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Millau, France
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Molsheim, France
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Montauban, France
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Montauban Cedex, France
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Montbeliard, France
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Montfermeil, France
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Montgeron, France
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Montigny Les Metz, France
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Montpellier, France
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Nancy, France
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Nans Les Pins, France
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Nantes, France
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Narbonne, France
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Nevers, France
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Nice, France
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Nimes Cedex 9, France
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Niort, France
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Nogent Sur Marne, France
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Ollioules, France
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Oloron Ste Marie, France
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Orleans, France
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Paris, France
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Paris Cedex 14, France
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Paris Cedex 15, France
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Perpignan Cedex, France
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Pessac, France
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Pezenas, France
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Poitiers, France
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Pontault Combault, France
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Pontivy, France
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Reims, France
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Reims Cedex, France
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Rennes, France
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Rouen, France
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Royan, France
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Rueil Malmaison, France
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Sarlat La Caneda, France
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Selestat, France
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Sens, France
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St Andre, France
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St Andre Les Vergers, France
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St Brieuc Cedex 1, France
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St Denis Cedex, France
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St Esteve Cedex, France
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St Etienne, France
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St Girons, France
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St Jean, France
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St Jean de Maurienne, France
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St Julien de Raz, France
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St Malo, France
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St Martin Boulogne, France
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St Martin D Heres, France
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St Orens de Gameville, France
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St Quentin, France
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Ste Clotilde Cedex, France
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Strasbourg, France
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Taden, France
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Tergnier, France
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Thionville, France
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Thonon Les Bains, France
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Thouars Cedex, France
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Toulon, France
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Toulouse, France
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Toulouse Cedex 3, France
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Tourcoing, France
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Tours, France
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Valence, France
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Valenciennes Cedex, France
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Venissieux, France
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Vienne, France
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Vierzon, France
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Villefranche Sur Saone, France
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Villefranche de Lauragais, France
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Villeurbanne, France
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
First 3 consecutive adults with COPD with at least a three month follow up, seen by pneumologist
Description
Inclusion Criteria:
- Adult patient who has a clinical visit for their usual follow-up.
- patient with COPD with at least a three month follow up
Exclusion Criteria:
- Current or history of asthma
- Current participation in an interventional clinical study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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1
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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To evaluate with sufficient precision and according to gender the determining independent factors of quality of life related to respiratory status of patient with moderate to severe COPD
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Alain Alain Castaigne, Medical Director, AstraZeneca
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2009
Primary Completion (Actual)
July 1, 2010
Study Completion (Actual)
July 1, 2010
Study Registration Dates
First Submitted
October 31, 2009
First Submitted That Met QC Criteria
November 3, 2009
First Posted (Estimate)
November 4, 2009
Study Record Updates
Last Update Posted (Estimate)
July 27, 2010
Last Update Submitted That Met QC Criteria
July 26, 2010
Last Verified
July 1, 2010
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NIS-RFR-DUM-2009/1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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