ID

31060

Beschreibung

Study of M2ES With Paclitaxel/Carboplatin (TC Regimen) in Advanced Non Small Cell Lung Cancer (NSCLC); ODM derived from: https://clinicaltrials.gov/show/NCT01099124

Link

https://clinicaltrials.gov/show/NCT01099124

Stichworte

  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.

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 NCT01099124

Eligibility Non Small Cell Lung Cancer NCT01099124

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. aged 18-70 years old;
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
2. patients with ⅲ/ⅳ nsclc confirmed by histopathology or cytology who ware naive or previous chemotherapy without tc regimen;
Beschreibung

Non-Small Cell Lung Carcinoma TNM clinical staging | Therapy naive | Prior Chemotherapy Without TC Regimen

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C3258246
UMLS CUI [2]
C0919936
UMLS CUI [3,1]
C1514457
UMLS CUI [3,2]
C0332288
UMLS CUI [3,3]
C4522122
3. no contraindication for chemotherapy;
Beschreibung

Medical contraindication Absent Chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0392920
4. ecog performance scale 0-2;
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
5. no history of anti-angiogenesis therapy;
Beschreibung

Antiangiogenesis therapy Absent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0281318
UMLS CUI [1,2]
C0332197
6. patients are voluntary to participate and sigh the informed contents.
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. concurrent use of other anti-cancer agents;
Beschreibung

Antineoplastic Agents

Datentyp

boolean

Alias
UMLS CUI [1]
C0003392
2. allergic history to m2es and biological agents;
Beschreibung

Hypersensitivity M2ES | Hypersensitivity Biological Factors

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C2985192
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0005515
3. pregnant or breast-feeding women;
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
4. with other malignancy;
Beschreibung

Cancer Other

Datentyp

boolean

Alias
UMLS CUI [1]
C1707251
5. with severe cardiopulmonary disease;
Beschreibung

Cor pulmonale Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0034072
UMLS CUI [1,2]
C0205082
6. uncontrolled brain metastasis patients;
Beschreibung

Metastatic malignant neoplasm to brain Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0220650
UMLS CUI [1,2]
C0205318
7. other conditions that are regarded for exclusion by the trialists.
Beschreibung

Condition Study Subject Participation Status Exclusion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C2828389

Ähnliche Modelle

Eligibility Non Small Cell Lung Cancer NCT01099124

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1. aged 18-70 years old;
boolean
C0001779 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma TNM clinical staging | Therapy naive | Prior Chemotherapy Without TC Regimen
Item
2. patients with ⅲ/ⅳ nsclc confirmed by histopathology or cytology who ware naive or previous chemotherapy without tc regimen;
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0919936 (UMLS CUI [2])
C1514457 (UMLS CUI [3,1])
C0332288 (UMLS CUI [3,2])
C4522122 (UMLS CUI [3,3])
Medical contraindication Absent Chemotherapy
Item
3. no contraindication for chemotherapy;
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
ECOG performance status
Item
4. ecog performance scale 0-2;
boolean
C1520224 (UMLS CUI [1])
Antiangiogenesis therapy Absent
Item
5. no history of anti-angiogenesis therapy;
boolean
C0281318 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
6. patients are voluntary to participate and sigh the informed contents.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Antineoplastic Agents
Item
1. concurrent use of other anti-cancer agents;
boolean
C0003392 (UMLS CUI [1])
Hypersensitivity M2ES | Hypersensitivity Biological Factors
Item
2. allergic history to m2es and biological agents;
boolean
C0020517 (UMLS CUI [1,1])
C2985192 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0005515 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
3. pregnant or breast-feeding women;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Cancer Other
Item
4. with other malignancy;
boolean
C1707251 (UMLS CUI [1])
Cor pulmonale Severe
Item
5. with severe cardiopulmonary disease;
boolean
C0034072 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Metastatic malignant neoplasm to brain Uncontrolled
Item
6. uncontrolled brain metastasis patients;
boolean
C0220650 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Condition Study Subject Participation Status Exclusion
Item
7. other conditions that are regarded for exclusion by the trialists.
boolean
C0348080 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

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