ID

31203

Descripción

FDG-PET Scan Response Guided Chemotherapy Strategy for Advanced Non-small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01170923

Link

https://clinicaltrials.gov/show/NCT01170923

Palabras clave

Versiones (1)
  1. 28/7/18 28/7/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

28 de julio de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Non-small Cell Lung Cancer NCT01170923

Inglés

Eligibility Non-small Cell Lung Cancer NCT01170923

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. histologically confirmed non-small cell carcinoma.
Descripción

Non-Small Cell Lung Carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007131
2. stage iiib (wet) or iv advanced nsclc.
Descripción

Non-Small Cell Lung Carcinoma Advanced TNM clinical staging

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0205179
UMLS CUI [1,3]
C3258246
3. no evidence of prior malignancies for 3 years except treated basal cell or squamous cell carcinoma of skin and carcinoma in situ of uterine cervix.
Descripción

Malignant Neoplasms Previous Absent | Exception Basal cell carcinoma Treated | Exception Squamous cell carcinoma of skin Treated | Exception Carcinoma in situ of uterine cervix Treated

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0205156
UMLS CUI [1,3]
C0332197
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007117
UMLS CUI [2,3]
C1522326
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0553723
UMLS CUI [3,3]
C1522326
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0851140
UMLS CUI [4,3]
C1522326
4. measurable disease by recist criteria.
Descripción

Measurable Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1513041
5. adequate organ function as follows.
Descripción

Organ function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678852
seum ast/alt < 2.5 x upper normal limit (unl) (if hepatic metastasis < 5 x unl)
Descripción

Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Relationship Secondary malignant neoplasm of liver

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201899
UMLS CUI [2]
C0201836
UMLS CUI [3,1]
C0439849
UMLS CUI [3,2]
C0494165
total bilirubin < 1.5 x unl
Descripción

Serum total bilirubin measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1278039
serum creatinine < 1.5 mg/dl
Descripción

Creatinine measurement, serum

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201976
absolute neutrophil count > 1500/ul
Descripción

Absolute neutrophil count

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0948762
platelet > 100,000/ul
Descripción

Platelet Count measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032181
hemoglobin > 9.0 g/dl
Descripción

Hemoglobin measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0518015
6. ecog performance status 0-1 7 age > 18
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
8. if previously treated with major surgery, it should be over at least 4 weeks. and if previously treated with radiotherapy, it should be over at least 2 weeks.
Descripción

Major surgery | Therapeutic radiology procedure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0679637
UMLS CUI [2]
C1522449
9. written consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. previous chemotherapy.
Descripción

Prior Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514457
2. symptomatic brain metastasis.
Descripción

Metastatic malignant neoplasm to brain Symptomatic

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0220650
UMLS CUI [1,2]
C0231220
3. concurrent severe medical illness.
Descripción

Illness Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205082
4. pregnancy and lactation.
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
5. if there are findings which may increase risk with chemotherapy or inhibit to analyze the result of clinical trial.
Descripción

Finding Chemotherapy At risk | Finding Preventing Analysis Research results

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0243095
UMLS CUI [1,2]
C0392920
UMLS CUI [1,3]
C1444641
UMLS CUI [2,1]
C0243095
UMLS CUI [2,2]
C1292733
UMLS CUI [2,3]
C0936012
UMLS CUI [2,4]
C0683954
uncontrolled diabetes mellitus.
Descripción

Diabetic - poor control

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0421258
Volver a la parte superior de la página

Similar models

Eligibility Non-small Cell Lung Cancer NCT01170923

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma
Item
1. histologically confirmed non-small cell carcinoma.
boolean
C0007131 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma Advanced TNM clinical staging
Item
2. stage iiib (wet) or iv advanced nsclc.
boolean
C0007131 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
Malignant Neoplasms Previous Absent | Exception Basal cell carcinoma Treated | Exception Squamous cell carcinoma of skin Treated | Exception Carcinoma in situ of uterine cervix Treated
Item
3. no evidence of prior malignancies for 3 years except treated basal cell or squamous cell carcinoma of skin and carcinoma in situ of uterine cervix.
boolean
C0006826 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])
C1522326 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0553723 (UMLS CUI [3,2])
C1522326 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0851140 (UMLS CUI [4,2])
C1522326 (UMLS CUI [4,3])
Measurable Disease
Item
4. measurable disease by recist criteria.
boolean
C1513041 (UMLS CUI [1])
Organ function
Item
5. adequate organ function as follows.
boolean
C0678852 (UMLS CUI [1])
Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Relationship Secondary malignant neoplasm of liver
Item
seum ast/alt < 2.5 x upper normal limit (unl) (if hepatic metastasis < 5 x unl)
boolean
C0201899 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0439849 (UMLS CUI [3,1])
C0494165 (UMLS CUI [3,2])
Serum total bilirubin measurement
Item
total bilirubin < 1.5 x unl
boolean
C1278039 (UMLS CUI [1])
Creatinine measurement, serum
Item
serum creatinine < 1.5 mg/dl
boolean
C0201976 (UMLS CUI [1])
Absolute neutrophil count
Item
absolute neutrophil count > 1500/ul
boolean
C0948762 (UMLS CUI [1])
Platelet Count measurement
Item
platelet > 100,000/ul
boolean
C0032181 (UMLS CUI [1])
Hemoglobin measurement
Item
hemoglobin > 9.0 g/dl
boolean
C0518015 (UMLS CUI [1])
ECOG performance status
Item
6. ecog performance status 0-1 7 age > 18
boolean
C1520224 (UMLS CUI [1])
Major surgery | Therapeutic radiology procedure
Item
8. if previously treated with major surgery, it should be over at least 4 weeks. and if previously treated with radiotherapy, it should be over at least 2 weeks.
boolean
C0679637 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Informed Consent
Item
9. written consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Prior Chemotherapy
Item
1. previous chemotherapy.
boolean
C1514457 (UMLS CUI [1])
Metastatic malignant neoplasm to brain Symptomatic
Item
2. symptomatic brain metastasis.
boolean
C0220650 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
Illness Severe
Item
3. concurrent severe medical illness.
boolean
C0221423 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
4. pregnancy and lactation.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Finding Chemotherapy At risk | Finding Preventing Analysis Research results
Item
5. if there are findings which may increase risk with chemotherapy or inhibit to analyze the result of clinical trial.
boolean
C0243095 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,3])
C0243095 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C0936012 (UMLS CUI [2,3])
C0683954 (UMLS CUI [2,4])
Diabetic - poor control
Item
uncontrolled diabetes mellitus.
boolean
C0421258 (UMLS CUI [1])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial