ID

12941

Descripción

SWOG-S9635 Fluorouracil Plus Ethynyluracil in Advanced Colorectal Cancer Not Responded to Fluorouracil; ODM derived from: https://clinicaltrials.gov/show/NCT00003254

Link

https://clinicaltrials.gov/show/NCT00003254

Palabras clave

Versiones (1)
  1. 7/1/16 7/1/16 -
Titular de derechos de autor

CC BY-NC 3.0

Subido en

7 de enero de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0
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Eligibility Colorectal Cancer NCT00003254

Inglés

Eligibility Colorectal Cancer NCT00003254

1 formularios  
Criteria
Descripción

Criteria

prior surgery required
Descripción

surgery

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0543467
no prior treatment for metastatic disease
Descripción

no prior treatment for metastatic disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027627
disease progression while on fluorouracil adjuvant therapy
Descripción

disease progression while on fluorouracil adjuvant therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0016360
bidimensionally measurable disease
Descripción

bidimensionally measurable disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1513041
age: over 18
Descripción

age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
performance status: swog 0-2
Descripción

performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1518965
hematopoietic: platelet count at least 100,000/mm3, absolute granulocyte count at least 1,500/mm3
Descripción

hematopoietic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005821
UMLS CUI [2]
C0857490
hepatic: bilirubin no greater than 1.5 times upper limit of normal (uln) sgot or sgpt no greater than 3 times uln (no greater than 5 times uln if liver involvement)
Descripción

hepatic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2]
C0201899
UMLS CUI [3]
C0201836
renal: creatinine clearance at least 50 ml/min
Descripción

renal

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0373595
other: must be able to swallow and retain oral medications no nutritional support by gastrostomy feeding tube or parenteral support no intractable vomiting or nausea
Descripción

other: must be able to swallow and retain oral medications no nutritional support by gastrostomy feeding tube or parenteral support no intractable vomiting or nausea

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0175795
patients with history of prior malignancy must be currently disease free and off all therapy for that malignancy
Descripción

malignancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
not pregnant or nursing fertile patients must use effective contraception
Descripción

not pregnant or nursing fertile patients must use effective contraception

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0700589
biologic therapy: no concurrent immunotherapy chemotherapy; at least 3 weeks since prior chemotherapy and recovered; no concurrent flucytosine; no other concurrent chemotherapy
Descripción

biologic therapy: no concurrent immunotherapy chemotherapy; at least 3 weeks since prior chemotherapy and recovered; no concurrent flucytosine; no other concurrent chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C0016278
endocrine therapy: no concurrent hormonal therapy
Descripción

endocrine therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279025
radiotherapy: prior adjuvant pelvic radiation or radiation to one area of recurrence allowed at least 4 weeks since prior radiotherapy and recovered total area of bone marrow irradiation must not exceed 25% no concurrent radiotherapy
Descripción

radiotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1522449
surgery: at least 2 weeks since prior surgery for colorectal cancer and recovered no prior resection of the stomach or small intestine
Descripción

surgery

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0543467
other: no other concurrent anticancer therapy
Descripción

other: no other concurrent anticancer therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0087111
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Similar models

Eligibility Colorectal Cancer NCT00003254

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
surgery
Item
prior surgery required
boolean
C0543467 (UMLS CUI [1])
no prior treatment for metastatic disease
Item
no prior treatment for metastatic disease
boolean
C0027627 (UMLS CUI [1])
disease progression while on fluorouracil adjuvant therapy
Item
disease progression while on fluorouracil adjuvant therapy
boolean
C0016360 (UMLS CUI [1])
bidimensionally measurable disease
Item
bidimensionally measurable disease
boolean
C1513041 (UMLS CUI [1])
age
Item
age: over 18
boolean
C0001779 (UMLS CUI [1])
performance status
Item
performance status: swog 0-2
boolean
C1518965 (UMLS CUI [1])
hematopoietic
Item
hematopoietic: platelet count at least 100,000/mm3, absolute granulocyte count at least 1,500/mm3
boolean
C0005821 (UMLS CUI [1])
C0857490 (UMLS CUI [2])
hepatic
Item
hepatic: bilirubin no greater than 1.5 times upper limit of normal (uln) sgot or sgpt no greater than 3 times uln (no greater than 5 times uln if liver involvement)
boolean
C1278039 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
renal
Item
renal: creatinine clearance at least 50 ml/min
boolean
C0373595 (UMLS CUI [1])
other: must be able to swallow and retain oral medications no nutritional support by gastrostomy feeding tube or parenteral support no intractable vomiting or nausea
Item
other: must be able to swallow and retain oral medications no nutritional support by gastrostomy feeding tube or parenteral support no intractable vomiting or nausea
boolean
C0175795 (UMLS CUI [1])
malignancy
Item
patients with history of prior malignancy must be currently disease free and off all therapy for that malignancy
boolean
C0006826 (UMLS CUI [1])
not pregnant or nursing fertile patients must use effective contraception
Item
not pregnant or nursing fertile patients must use effective contraception
boolean
C0032961 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
biologic therapy: no concurrent immunotherapy chemotherapy; at least 3 weeks since prior chemotherapy and recovered; no concurrent flucytosine; no other concurrent chemotherapy
Item
biologic therapy: no concurrent immunotherapy chemotherapy; at least 3 weeks since prior chemotherapy and recovered; no concurrent flucytosine; no other concurrent chemotherapy
boolean
C0392920 (UMLS CUI [1])
C0016278 (UMLS CUI [2])
endocrine therapy
Item
endocrine therapy: no concurrent hormonal therapy
boolean
C0279025 (UMLS CUI [1])
radiotherapy
Item
radiotherapy: prior adjuvant pelvic radiation or radiation to one area of recurrence allowed at least 4 weeks since prior radiotherapy and recovered total area of bone marrow irradiation must not exceed 25% no concurrent radiotherapy
boolean
C1522449 (UMLS CUI [1])
surgery
Item
surgery: at least 2 weeks since prior surgery for colorectal cancer and recovered no prior resection of the stomach or small intestine
boolean
C0543467 (UMLS CUI [1])
other: no other concurrent anticancer therapy
Item
other: no other concurrent anticancer therapy
boolean
C0087111 (UMLS CUI [1])
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