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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00831909
Other study ID # NIS-OEU-DUM-2008/1
Secondary ID
Status Completed
Phase N/A
First received January 28, 2009
Last updated August 9, 2010
Start date January 2009
Est. completion date July 2010

Study information

Verified date August 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Spain: Ethics CommitteeBelgium: Institutional Review BoardFrance: French Data Protection AuthorityGermany: Ethics CommissionGreece: National Organization of MedicinesItaly: Ethics CommitteePortugal: Ethics Committee for Clinical ResearchTurkey: Ministry of Health
Study type Observational

Clinical Trial Summary

To provide accurate and reliable information regarding NSCLC clinical management across European countries in order to detect unmet medical needs of this disease in terms of: patient and hospital characteristics; diagnostic and treatment approaches: initial and subsequent, follow-up patterns in clinical management; outcomes: symptoms, death, functionality, quality of life; use of resources and burden on patients and health care systems.


Recruitment information / eligibility

Status Completed
Enrollment 3513
Est. completion date July 2010
Est. primary completion date July 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Confirmed NSCLC diagnosis (e.g. bronchoscope or FNAB), all stages, men and women, attending the responsible department of treating this type of patients for the first time between January 1st, 2009 and March 31st, 2009.

- For PRO sub-sample: ability to read and write since they will be asked to participate in the PRO part of the study. Selection will not be based on the disease stage of each patient, in order to avoid a selection bias.

Exclusion Criteria:

- According to the study design there will not be any exclusion criteria in order to provide a high external validity and to obtain the most accurate real daily practice information.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium Research Site Antwerpen
Belgium Research Site Bruxelles
Belgium Research Site Genk
Belgium Research Site Herstal
Belgium Research Site Liege
France Research Site Aix En Provence Cedex 1
France Research Site Ambilly
France Research Site Antibes Cedex
France Research Site Aulnay Sous Bois Cedex
France Research Site Bar Le Duc Cedex
France Research Site Beauvais Cedex
France Research Site Beuvry
France Research Site Bordeaux
France Research Site Brest Cedex 2
France Research Site Cahors Cedex 9
France Research Site Castelnau Le Lez
France Research Site Chalon Sur Saone
France Research Site Chauny Cedex
France Research Site Chevilly Larue Cedex
France Research Site Cholet Cedex
France Research Site Clamart Cedex
France Research Site Colmar Cedex
France Research Site Compiegne Cedex
France Research Site Coulommiers Cedex
France Research Site Denain Cedex
France Research Site Dijon Cedex
France Research Site Douai Cedex
France Research Site Draguignan Cedex
France Research Site Epinal Cedex
France Research Site Flers Cedex
France Research Site Givors Cedex
France Research Site Granville Cedex
France Research Site Grasse Cedex
France Research Site Guingamp Cedex
France Research Site Hyeres
France Research Site Jonzac Cedex
France Research Site La Ferte Bernard Cedex
France Research Site La Rochelle Cedex 1
France Research Site La Tronche
France Research Site Le Mans Cedex 9
France Research Site Lievin Cedex
France Research Site Limoges Cedex 1
France Research Site Longjumeau Cedex
France Research Site Lyon Cedex 04
France Research Site Lyon Cedex 08
France Research Site Mantes La Jolie Cedex
France Research Site Martigues Cedex
France Research Site Meaux Cedex
France Research Site Metz Cedex 01
France Research Site Metz Cedex 03
France Research Site Metz Tessy
France Research Site Mont de Marsan Cedex
France Research Site Mont St Martin
France Research Site Montpellier
France Research Site Montpellier Cedex 5
France Research Site Moulins Cedex
France Research Site Mulhouse Cedex
France Research Site Mulhouse Cedex 1
France Research Site Nancy
France Research Site Nevers Cedex
France Research Site Nice
France Research Site Nimes Cedex 9
France Research Site Oloron Ste Marie Cedex
France Research Site Paris Cedex 04
France Research Site Paris Cedex 05
France Research Site Paris Cedex 12
France Research Site Paris Cedex 15
France Research Site Perpignan Cedex
France Research Site Pierre Benite Cedex
France Research Site Pontoise
France Research Site Quimper Cedex
France Research Site Rambouillet Cedex
France Research Site Reims Cedex
France Research Site Rennes Cedex
France Research Site Saverne Cedex
France Research Site Soissons Cedex
France Research Site St Aubin Les Elbeuf
France Research Site St Priest En Jarez Cedex
France Research Site Strasbourg
France Research Site Strasbourg Cedex
France Research Site Thonon Les Bains Cedex
France Research Site Toulon Armees
France Research Site Toulon Cedex
France Research Site Toulouse Cedex 3
France Research Site Toulouse Cedex 9
France Research Site Valence Cedex 9
France Research Site Vandoeuvre Les Nancy Cedex
France Research Site Verdun Cedex
France Research Site Vesoul Cedex
France Research Site Vire Cedex
Germany Research Site Essen Nordrhein-Westfalen
Germany Research Site Gro?hansdorf Schleswig-Holstein
Germany Research Site Halle Sachsen-Anhalt
Germany Research Site Hamburg-Harburg Hamburg
Germany Research Site Heidelberg Baden W?rttemberg
Germany Research Site Hemer Nordrhein-Westfalen
Germany Research Site Leipzig Sachsen
Germany Research Site Lowenstein Baden-W?rttemberg
Germany Research Site Munchen-Gauting Bayern
Germany Research Site Ulm Baden-W?rtemberg
Greece Research Site Athens
Greece Research Site Heraklio Crete
Greece Research Site Ioannina
Greece Research Site Patra
Greece Research Site Piraeus
Greece Research Site Thessaloniki
Italy Research Site Bologna
Italy Research Site Brindisi
Italy Research Site Carpi
Italy Research Site Cattolica
Italy Research Site Cesena
Italy Research Site Cremona
Italy Research Site Faenza
Italy Research Site Fano
Italy Research Site Legnano
Italy Research Site Lido di Camaiore
Italy Research Site Lugo
Italy Research Site Mantova
Italy Research Site Meldola
Italy Research Site Milano
Italy Research Site Napoli
Italy Research Site Parma
Italy Research Site Perugia
Italy Research Site Ravenna
Italy Research Site Rimini
Italy Research Site S. Giovanni Rotondo
Italy Research Site Saronno
Italy Research Site Sondrio
Italy Research Site Verona
Portugal Research Site Lisboa
Portugal Research Site Ponta Delgada
Portugal Research Site Porto
Portugal Research Site Sta.Ma Feira
Portugal Research Site V.N: de Gaia
Spain Research Site A Coruna
Spain Research Site Alicante
Spain Research Site Barcelona
Spain Research Site Cabuenes
Spain Research Site Calella
Spain Research Site Castellon
Spain Research Site Cordoba
Spain Research Site Cuenca
Spain Research Site Elche
Spain Research Site Jaen
Spain Research Site Leon
Spain Research Site Lerida
Spain Research Site Madrid
Spain Research Site Malaga
Spain Research Site Manacor
Spain Research Site Mataro
Spain Research Site Melilla
Spain Research Site Oviedo
Spain Research Site Palma de Mallorca
Spain Research Site Pamplona
Spain Research Site Puerto Real
Spain Research Site Sagunto
Spain Research Site Salamanca
Spain Research Site Sevilla
Spain Research Site Sta Cruz de Tenerife Tenerife
Spain Research Site Tenerife
Spain Research Site Tudela
Spain Research Site Valencia
Spain Research Site Xativa
Spain Research Site Zaragoza
Turkey Research Site Adana
Turkey Research Site Ankara
Turkey Research Site Gaziantep
Turkey Research Site Istanbul
Turkey Research Site Izmir
Turkey Research Site Konya

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Countries where clinical trial is conducted

Belgium,  France,  Germany,  Greece,  Italy,  Portugal,  Spain,  Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary To provide accurate, reliable information on NSCLC clinical management across European countries in order to detect unmet medical needs of this disease 1 year follow up No
Secondary To assess the differences in patient characteristics, disease stage (differentiating between non-advanced disease, locally advanced disease, metastatic disease), and in clinical management across European countries. 1 year follow up No
Secondary To detect differences in clinical outcomes and related factors among countries. 1 year follow up No
Secondary To identify factors associated with clinical outcomes (patient, disease stage and clinical management related factors): predictive modelling for improved patient outcome. 1 year follow up No
Secondary To identify factors associated with the different levels of functional status and quality of life. 1 year follow up No
Secondary To compare the use of health care resources among countries. 1 year follow up No
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