Information:
Error:
ID
12941
Description
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
Keywords
Versions (1)
- 1/7/16 1/7/16 -
Copyright Holder
CC BY-NC 3.0
Uploaded on
January 7, 2016
DOI
To request one please log in.
License
Creative Commons BY-NC 3.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
Eligibility Colorectal Cancer NCT00003254
Eligibility Colorectal Cancer NCT00003254
- StudyEvent: Eligibility
Similar models
Eligibility Colorectal Cancer NCT00003254
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
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])
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])
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])
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])
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])