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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00002823




Registration number
NCT00002823
Ethics application status
Date submitted
1/11/1999
Date registered
11/03/2004
Date last updated
28/03/2013

Titles & IDs
Public title
Combination Chemotherapy Compared With No Treatment Following Surgery in Treating Patients With Non-small Cell Lung Cancer
Scientific title
A LARGE-SCALE TRIAL EVALUATING ADJUVANT CHEMOTHERAPY AFTER CURATIVE RESECTION OF NON-SMALL CELL LUNG CANCER
Secondary ID [1] 0 0
FRE-IALT
Secondary ID [2] 0 0
CDR0000065002
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Lung Cancer 0 0
Condition category
Condition code
Cancer 0 0 0 0
Lung - Mesothelioma
Cancer 0 0 0 0
Lung - Non small cell
Cancer 0 0 0 0
Lung - Small cell

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Comparator / control treatment
Control group

Outcomes

Eligibility
Key inclusion criteria
DISEASE CHARACTERISTICS: Histologically documented non-small cell lung cancer Any non-small cell histology eligible Pathologic stage I/II/III disease that is completely resected with microscopically clear margins within 60 days of entry (30 days preferred)

PATIENT CHARACTERISTICS: Age: 18 to 75 Performance status: Not specified Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified Other: No clear contraindication to chemotherapy No second malignancy except: Nonmelanomatous skin cancer Carcinoma in situ of the cervix

PRIOR CONCURRENT THERAPY: Biologic therapy: No prior immunotherapy Chemotherapy: No prior chemotherapy Endocrine therapy: Not specified Radiotherapy: No prior thoracic radiotherapy Surgery: Complete resection required prior to entry
Minimum age
18 Years
Maximum age
75 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,SA,VIC
Recruitment hospital [1] 0 0
South Eastern Sydney Area Health Service - Randwick
Recruitment hospital [2] 0 0
Royal Adelaide Hospital - Adelaide
Recruitment hospital [3] 0 0
Peter MacCallum Cancer Institute - East Melbourne
Recruitment hospital [4] 0 0
Western Hospital - Melbourne
Recruitment hospital [5] 0 0
Alfred Hospital - Melbourne
Recruitment hospital [6] 0 0
Royal Melbourne Hospital - Parkville
Recruitment postcode(s) [1] 0 0
2031 - Randwick
Recruitment postcode(s) [2] 0 0
5000 - Adelaide
Recruitment postcode(s) [3] 0 0
8006 - East Melbourne
Recruitment postcode(s) [4] 0 0
3011 - Melbourne
Recruitment postcode(s) [5] 0 0
3181 - Melbourne
Recruitment postcode(s) [6] 0 0
3050 - Parkville
Recruitment outside Australia
Country [1] 0 0
United States of America
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Florida
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United States of America
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Massachusetts
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Argentina
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Buenos Aires
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Austria
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Vienna
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Belgium
State/province [5] 0 0
Brugge
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Belgium
State/province [6] 0 0
Edegem
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Belgium
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Leuven
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Belgium
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Ronse
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Belgium
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Zottegem
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Brazil
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Rio Grande do Sul
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Brazil
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Rio de Janeiro
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Brazil
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Rio De Janeiro
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Brazil
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Sao Paulo
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Chile
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Santiago
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Colombia
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Bogota
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Czech Republic
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Prague (Praha)
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Egypt
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Cairo
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Former Yugoslavia
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Belgrade
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France
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Angers
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France
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Armentieres
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France
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Aulnay Sous Bois
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France
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Aurillac
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France
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Bagneux
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France
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Beauvais
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France
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Bobigny
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France
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Bois Guillaume (Rouen)
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Bordeaux
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Caen
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Cannes
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France
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Chartres
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France
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Clamart
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Compiegne
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Creteil
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Dijon
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France
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Etampes
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Grasse
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Lagny
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Le Havre
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Lille
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Lyon
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Marseille
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Mayenne
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Metz
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Meudon-La-Foret
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Montpellier
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Neuilly sur Seine
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Nice
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Paris
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Pau
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Poitiers
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Rennes
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Saint-Brieuc
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Sarcelles
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Sens
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Strasbourg
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Troyes
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Vandoeuvre-les-Nancy
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Villejuif
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Greece
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Crete
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Athens
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Piraeus
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Rio Patras
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Greece
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Thessaloniki
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Israel
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Rehovot
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Israel
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Tel-Aviv
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Milano
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Naples
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Palermo
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Rimini
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Rome
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Italy
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Torino
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Italy
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Turin
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Italy
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Udine
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Italy
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Verona
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Japan
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Osaka
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Lithuania
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Vilnius
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Macedonia, The Former Yugoslav Republic of
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Skopje
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Morocco
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Rabat
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Norway
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Tromso
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Quezon City Diliman
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Bialystok
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Wroclaw
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Zdunowo
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Portugal
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Lisbon (Lisboa)
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Slovenia
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Ljubljana
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South Africa
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Cape Town
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South Africa
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Johannesburg
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Spain
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Barcelona
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Spain
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Granada
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Spain
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Valencia
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Sweden
State/province [92] 0 0
Gothenburg (Goteborg)
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Sweden
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Linkoping
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Sweden
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Lund
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Sweden
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Stockholm
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Sweden
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Uppsala
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Switzerland
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Basel
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Switzerland
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Bellinzona
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Chur
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Switzerland
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Geneva
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Switzerland
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Luzern (Lucerne)
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Switzerland
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Zurich
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Tunisia
State/province [103] 0 0
Monastir

Funding & Sponsors
Primary sponsor type
Other
Name
Gustave Roussy, Cancer Campus, Grand Paris
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Thierry L. Le Chevalier, MD
Address 0 0
Gustave Roussy, Cancer Campus, Grand Paris
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents