ID

38383

Descripción

Docetaxel +/- Suramin in 2nd Line Advanced Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01671332

Link

https://clinicaltrials.gov/show/NCT01671332

Palabras clave

Versiones (1)
  1. 14/10/19 14/10/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

14 de octubre de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Carcinoma, Non Small Cell Lung NCT01671332

Inglés

Eligibility Carcinoma, Non Small Cell Lung NCT01671332

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
pathologically proven diagnosis of non-small cell lung cancer
Descripción

Non-Small Cell Lung Carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007131
documented disease progression after first-line chemotherapy for non-small cell lung cancer
Descripción

Disease Progression | First line Chemotherapy Non-Small Cell Lung Carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0242656
UMLS CUI [2,1]
C1708063
UMLS CUI [2,2]
C0392920
UMLS CUI [2,3]
C0007131
stable and treated cns metastasis is allowed
Descripción

CNS metastases Stable Treated

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0686377
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C1522326
radiation must be completed at least 2 weeks prior to starting protocol treatment
Descripción

Therapeutic radiology procedure Completed

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0205197
major surgery must be completed at least 4 weeks prior to starting protocol treatment
Descripción

Major surgery Completed

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0679637
UMLS CUI [1,2]
C0205197
ecog performance status 0-2
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
sexually active patients must use adequate contraception
Descripción

Patients Sexually active Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0241028
UMLS CUI [1,3]
C0700589
adequate bone marrow function
Descripción

Bone Marrow function

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
adequate renal function
Descripción

Renal function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232804
adequate liver function
Descripción

Liver function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232741
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe hypersensitivity reaction to docetaxel
Descripción

Severe allergy Docetaxel

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2945656
UMLS CUI [1,2]
C0246415
pre-existing grade 3 or 4 neuropathy
Descripción

Neuropathy Pre-existing CTCAE Grades

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0442874
UMLS CUI [1,2]
C2347662
UMLS CUI [1,3]
C1516728
women who are pregnant or breastfeeding
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
uncontrolled intercurrent illness
Descripción

Comorbidity Uncontrolled

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205318
receipt of 3 or more prior chemotherapy regimens
Descripción

Prior Chemotherapy Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1514457
UMLS CUI [1,2]
C1265611
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Similar models

Eligibility Carcinoma, Non Small Cell Lung NCT01671332

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma
Item
pathologically proven diagnosis of non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
Disease Progression | First line Chemotherapy Non-Small Cell Lung Carcinoma
Item
documented disease progression after first-line chemotherapy for non-small cell lung cancer
boolean
C0242656 (UMLS CUI [1])
C1708063 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
C0007131 (UMLS CUI [2,3])
CNS metastases Stable Treated
Item
stable and treated cns metastasis is allowed
boolean
C0686377 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C1522326 (UMLS CUI [1,3])
Therapeutic radiology procedure Completed
Item
radiation must be completed at least 2 weeks prior to starting protocol treatment
boolean
C1522449 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
Major surgery Completed
Item
major surgery must be completed at least 4 weeks prior to starting protocol treatment
boolean
C0679637 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
ECOG performance status
Item
ecog performance status 0-2
boolean
C1520224 (UMLS CUI [1])
Patients Sexually active Contraceptive methods
Item
sexually active patients must use adequate contraception
boolean
C0030705 (UMLS CUI [1,1])
C0241028 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
Bone Marrow function
Item
adequate bone marrow function
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
Renal function
Item
adequate renal function
boolean
C0232804 (UMLS CUI [1])
Liver function
Item
adequate liver function
boolean
C0232741 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Severe allergy Docetaxel
Item
severe hypersensitivity reaction to docetaxel
boolean
C2945656 (UMLS CUI [1,1])
C0246415 (UMLS CUI [1,2])
Neuropathy Pre-existing CTCAE Grades
Item
pre-existing grade 3 or 4 neuropathy
boolean
C0442874 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
C1516728 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
women who are pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Comorbidity Uncontrolled
Item
uncontrolled intercurrent illness
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Prior Chemotherapy Quantity
Item
receipt of 3 or more prior chemotherapy regimens
boolean
C1514457 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
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