- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00191126
Randomized Phase III Trial of Surgery Alone or Surgery Plus Preoperative Gemcitabine-Cisplatin in Early Stages NSCLC
10. september 2019 opdateret af: Eli Lilly and Company
Randomized Phase III Trial of Surgery Alone or Surgery Plus Preoperative Gemcitabine-Cisplatin in Clinical Early Stages(T2N0, T1 - 2N1, T3N0 AND T3N1) Non-Small Cell Lung Cancer (NSCLC)
Preoperative chemotherapy is considered to play a role in early stage non small cell lung cancer (NSCLC) .The use of preoperative Cisplatin/Gemcitabine chemotherapy has proven feasible and without excessive morbidity or mortality in the Phase II setting.
The aim of the present Phase III study is to determine whether 3 cycles of preoperative chemotherapy with Cisplatin/Gemcitabine improves progression free survival of NSCLC patients versus surgery alone.
Postoperative chemotherapy will not be utilized in this Phase III trial.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
263
Fase
- Fase 3
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Leuven, Belgien
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Liege, Belgien
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Sarajevo, Bosnien-Hercegovina
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Sofia, Bulgarien
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Varna, Bulgarien
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Cairo, Egypten
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Tallin, Estland
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Bologna, Italien
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Chieti, Italien
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L'Aquila, Italien
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Milano, Italien
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Napoli, Italien
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Padova, Italien
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Perugia, Italien
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Pisa, Italien
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Roma, Italien
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Siena, Italien
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Teramo, Italien
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Torino, Italien
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Verona, Italien
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Kaunas, Litauen
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Klaipedos, Litauen
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Vilnius, Litauen
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Warszawa, Polen
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Bucuresti, Rumænien
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Cluj, Rumænien
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Riyadh, Saudi Arabien
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Bratislava, Slovakiet
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Kosice, Slovakiet
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Helsingborg, Sverige
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Malmo, Sverige
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Taichung, Taiwan
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Grosshansdorf, Tyskland
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Loewenstein, Tyskland
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Nurnberg, Tyskland
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Ulm, Tyskland
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Pecs, Ungarn
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician.
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Main inclusion Criteria:
- Must have pathologic documentation of non-small cell lung cancer, IB, II, IIIA.
- ECOG Performance Status of 0 - 1
- Bidimensionally measurable disease or evaluable disease
- Adequate organ function
Main exclusion Criteria:
- Have greater than Grade 1 neuropathy - motor/sensory
- Significant history of cardiac disease
- Pleural effusion
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: B
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kirurgi
1250 mg/m2, IV, day 1 and 8, q 21 days x 3 cycles
Andre navne:
75 mg/m2, IV, q 21 days x 3 cycles
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Andet: EN
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kirurgi
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
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Progression free survival
Tidsramme: baseline to measure progressive disease
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baseline to measure progressive disease
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Sekundære resultatmål
Resultatmål |
Tidsramme |
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To compare the survival and sites of relapse in the two study arms.
Tidsramme: baseline to progressive disease
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baseline to progressive disease
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Pharmacology toxicity
Tidsramme: every cycle
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every cycle
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Svarprocent
Tidsramme: baseline til målt progressiv sygdom
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baseline til målt progressiv sygdom
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Pathologic response rate of tissue samples
Tidsramme: baseline, post chemotherapy, post surgery
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baseline, post chemotherapy, post surgery
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Hjælpsomme links
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. september 2000
Primær færdiggørelse (Faktiske)
1. september 2007
Studieafslutning (Faktiske)
1. september 2007
Datoer for studieregistrering
Først indsendt
12. september 2005
Først indsendt, der opfyldte QC-kriterier
12. september 2005
Først opslået (Skøn)
19. september 2005
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
12. september 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
10. september 2019
Sidst verificeret
1. september 2019
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Luftvejssygdomme
- Neoplasmer
- Lungesygdomme
- Neoplasmer efter sted
- Neoplasmer i luftvejene
- Thoracale neoplasmer
- Karcinom, bronkogent
- Bronkiale neoplasmer
- Lungeneoplasmer
- Karcinom, ikke-småcellet lunge
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Anti-infektionsmidler
- Antivirale midler
- Enzymhæmmere
- Antimetabolitter, Antineoplastisk
- Antimetabolitter
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Gemcitabin
Andre undersøgelses-id-numre
- 3532 (Andet bevillings-/finansieringsnummer: The Lundbeck Foundation)
- B9E-MC-S132 (Anden identifikator: Eli Lilly and Company)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Ja
IPD-planbeskrivelse
Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.
IPD-delingstidsramme
Data are available 6 months after the primary publication and approval of the indication studied in the US and EU, whichever is later.
Data will be indefinitely available for requesting.
IPD-delingsadgangskriterier
A research proposal must be approved by an independent review panel and researchers must sign a data sharing agreement.
IPD-deling Understøttende informationstype
- Studieprotokol
- Statistisk analyseplan (SAP)
- Klinisk undersøgelsesrapport (CSR)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Ikke-småcellet lungekræft
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AHS Cancer Control AlbertaCross Cancer InstituteAfsluttetOmfattende Stage Small Cel Lung CancerCanada
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Universitaire Ziekenhuizen KU LeuvenUkendtLymfom | Hodgkin lymfom | Non-Hodgkin lymfom (follikulært, diffust B-cel lymfom, PTLD og Mantle Cel lymfom)Belgien
Kliniske forsøg med kirurgi
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Diakonessenhuis, UtrechtRekrutteringLivskvalitet | Søvnapnø, obstruktivHolland
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Royal Surrey County Hospital NHS Foundation TrustUkendtLivmoderhalskræft | Æggelederkræft | Peritoneal kræft | Neoplasma i æggestokkene | Ovarie neoplasma epitelialDet Forenede Kongerige
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The Second Hospital of Shandong UniversityRekrutteringLungekræft | Kirurgi | ERASKina
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University of Colorado, DenverRekrutteringForbedret restitution efter operation | Gynækologisk sygdomForenede Stater
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University Hospital, GrenobleAfsluttet
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Grupo Español de Rehabilitación MultimodalInstituto de Salud Carlos III; Instituto de Investigación Sanitaria AragónRekrutteringStørre operationSpanien
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ARCAGY/ GINECO GROUPRekrutteringOvariekræft Stadium IIIC | Ovariekræft Stadium IV | Ovariekræft Stadium IIIbFrankrig
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Bournemouth UniversityStryker Orthopaedics; Nuffield Health Bournemouth; Orthopaedic Research InstituteRekrutteringSlidgigt, HofteDet Forenede Kongerige
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University of Illinois at ChicagoIkke rekrutterer endnuProstata hyperplasi
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Medacta International SARekrutteringRekonstruktion af forreste korsbånd (ACL).Østrig, Tyskland