ID

31059

Beschreibung

A Trial of Paclitaxel (Genexol®) and Cisplatin Versus Paclitaxel Loaded Polymeric Micelle (Genexol-PM®) and Cisplatin in Advanced Non Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01023347

Link

https://clinicaltrials.gov/show/NCT01023347

Stichworte

Versionen (1)
  1. 16.07.18 16.07.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

16. Juli 2018

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Non Small Cell Lung Cancer NCT01023347

Englisch

Eligibility Non Small Cell Lung Cancer NCT01023347

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histological or cytological evidence of locally advanced, metastatic or recurrent nsclc (stage iiib or iv)
Beschreibung

Non-Small Cell Lung Carcinoma Advanced Locally TNM clinical staging | Non-small cell lung cancer metastatic TNM clinical staging | Non-small cell lung cancer recurrent TNM clinical staging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0205179
UMLS CUI [1,3]
C1517927
UMLS CUI [1,4]
C3258246
UMLS CUI [2,1]
C0278987
UMLS CUI [2,2]
C3258246
UMLS CUI [3,1]
C0278517
UMLS CUI [3,2]
C3258246
at least one measurable lesion(s) by recist criteria
Beschreibung

Measurable Disease Quantity

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C1265611
no previous palliative chemotherapy
Beschreibung

Prior Chemotherapy Palliative Absent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C1285530
UMLS CUI [1,3]
C0332197
age 18 or higher.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
ecog ps 0-2
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
life expectancy of at least 3 months.
Beschreibung

Life Expectancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0023671
adequate hematologic, hepatic, renal function
Beschreibung

Hematologic function | Liver function | Renal function

Datentyp

boolean

Alias
UMLS CUI [1]
C0221130
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0232804
adequate bone marrow function (≥ anc 1,500/ul, ≥ platelet 100,000/ul)
Beschreibung

Bone Marrow function | Absolute neutrophil count | Platelet Count measurement

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
UMLS CUI [2]
C0948762
UMLS CUI [3]
C0032181
adequate liver function (≤ total bilirubin ≤ 1.5 upper normal limit, ≤ ast/alt x 2.5 upper normal limit, alkaline phosphatase ≤ 2.5 upper normal limit)
Beschreibung

Liver function | Serum total bilirubin measurement | Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Alkaline phosphatase measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C1278039
UMLS CUI [3]
C0201899
UMLS CUI [4]
C0201836
UMLS CUI [5]
C0201850
adequate renal function (≤ serum creatinine 1.5 mg/dl)
Beschreibung

Renal function | Creatinine measurement, serum

Datentyp

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0201976
written informed consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
no prior chemotherapy for nsclc
Beschreibung

Prior Chemotherapy Non-Small Cell Lung Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C0007131
patients with malignancies (other than nsclc), except for adequately treated nonmelanoma skin cancer or in situ carcinoma of the cervix.
Beschreibung

Malignant Neoplasms | Exception Non-Small Cell Lung Carcinoma | Exception Skin carcinoma Treated | Exception Carcinoma in situ of uterine cervix Treated

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007131
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0699893
UMLS CUI [3,3]
C1522326
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0851140
UMLS CUI [4,3]
C1522326
peripheral neuropathy ≥ grade 2 (nci ctc, version 3.0)
Beschreibung

Peripheral Neuropathy CTCAE Grades

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0031117
UMLS CUI [1,2]
C1516728
clinically significant cardiac disease (medically uncontrollable heart disease)
Beschreibung

Heart Disease Control Unsuccessful

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0243148
UMLS CUI [1,3]
C1272705
active infection or other serious medical illness
Beschreibung

Communicable Disease | Illness Serious

Datentyp

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2,1]
C0221423
UMLS CUI [2,2]
C0205404
contraindication to any drug contained in the chemotherapy regimen
Beschreibung

Medical contraindication Pharmaceutical Preparations Chemotherapy Regimen

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0392920
pregnant or lactating women were excluded.
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Non Small Cell Lung Cancer NCT01023347

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma Advanced Locally TNM clinical staging | Non-small cell lung cancer metastatic TNM clinical staging | Non-small cell lung cancer recurrent TNM clinical staging
Item
histological or cytological evidence of locally advanced, metastatic or recurrent nsclc (stage iiib or iv)
boolean
C0007131 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C1517927 (UMLS CUI [1,3])
C3258246 (UMLS CUI [1,4])
C0278987 (UMLS CUI [2,1])
C3258246 (UMLS CUI [2,2])
C0278517 (UMLS CUI [3,1])
C3258246 (UMLS CUI [3,2])
Measurable Disease Quantity
Item
at least one measurable lesion(s) by recist criteria
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Prior Chemotherapy Palliative Absent
Item
no previous palliative chemotherapy
boolean
C1514457 (UMLS CUI [1,1])
C1285530 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Age
Item
age 18 or higher.
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ecog ps 0-2
boolean
C1520224 (UMLS CUI [1])
Life Expectancy
Item
life expectancy of at least 3 months.
boolean
C0023671 (UMLS CUI [1])
Hematologic function | Liver function | Renal function
Item
adequate hematologic, hepatic, renal function
boolean
C0221130 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Bone Marrow function | Absolute neutrophil count | Platelet Count measurement
Item
adequate bone marrow function (≥ anc 1,500/ul, ≥ platelet 100,000/ul)
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0948762 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
Liver function | Serum total bilirubin measurement | Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Alkaline phosphatase measurement
Item
adequate liver function (≤ total bilirubin ≤ 1.5 upper normal limit, ≤ ast/alt x 2.5 upper normal limit, alkaline phosphatase ≤ 2.5 upper normal limit)
boolean
C0232741 (UMLS CUI [1])
C1278039 (UMLS CUI [2])
C0201899 (UMLS CUI [3])
C0201836 (UMLS CUI [4])
C0201850 (UMLS CUI [5])
Renal function | Creatinine measurement, serum
Item
adequate renal function (≤ serum creatinine 1.5 mg/dl)
boolean
C0232804 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Prior Chemotherapy Non-Small Cell Lung Carcinoma
Item
no prior chemotherapy for nsclc
boolean
C1514457 (UMLS CUI [1,1])
C0007131 (UMLS CUI [1,2])
Malignant Neoplasms | Exception Non-Small Cell Lung Carcinoma | Exception Skin carcinoma Treated | Exception Carcinoma in situ of uterine cervix Treated
Item
patients with malignancies (other than nsclc), except for adequately treated nonmelanoma skin cancer or in situ carcinoma of the cervix.
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007131 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0699893 (UMLS CUI [3,2])
C1522326 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0851140 (UMLS CUI [4,2])
C1522326 (UMLS CUI [4,3])
Peripheral Neuropathy CTCAE Grades
Item
peripheral neuropathy ≥ grade 2 (nci ctc, version 3.0)
boolean
C0031117 (UMLS CUI [1,1])
C1516728 (UMLS CUI [1,2])
Heart Disease Control Unsuccessful
Item
clinically significant cardiac disease (medically uncontrollable heart disease)
boolean
C0018799 (UMLS CUI [1,1])
C0243148 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Communicable Disease | Illness Serious
Item
active infection or other serious medical illness
boolean
C0009450 (UMLS CUI [1])
C0221423 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
Medical contraindication Pharmaceutical Preparations Chemotherapy Regimen
Item
contraindication to any drug contained in the chemotherapy regimen
boolean
C1301624 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnant or lactating women were excluded.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video