Informations:
Erreur:
ID
28286
Description
Bispecific Antibody in Finding Tumor Cells in Patients With Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00895323
Lien
https://clinicaltrials.gov/show/NCT00895323
Mots-clés
Versions (1)
- 02/01/2018 02/01/2018 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
2 janvier 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
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Eligibility Colorectal Cancer NCT00895323
Eligibility Colorectal Cancer NCT00895323
- StudyEvent: Eligibility
Similar models
Eligibility Colorectal Cancer NCT00895323
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Colorectal Carcinoma
Item
histologically confirmed colorectal cancer
boolean
C0009402 (UMLS CUI [1])
Disease Documentation Radiologic
Item
radiological documentation of disease is preferred, but not required
boolean
C0012634 (UMLS CUI [1,1])
C0920316 (UMLS CUI [1,2])
C0205483 (UMLS CUI [1,3])
C0920316 (UMLS CUI [1,2])
C0205483 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Karnofsky Performance Status
Item
karnofsky performance status 70-100%
boolean
C0206065 (UMLS CUI [1])
Life Expectancy
Item
life expectancy ≥ 3 months
boolean
C0023671 (UMLS CUI [1])
White Blood Cell Count procedure
Item
wbc ≥ 3,000/mm³
boolean
C0023508 (UMLS CUI [1])
Neutrophil count
Item
neutrophil count ≥ 1,500/mm³
boolean
C0200633 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count ≥ 100,000/mm³
boolean
C0032181 (UMLS CUI [1])
Serum creatinine normal
Item
serum creatinine normal
boolean
C0438244 (UMLS CUI [1])
Serum total bilirubin measurement
Item
bilirubin ≤ 1.5 times upper limit of normal (uln)
boolean
C1278039 (UMLS CUI [1])
Aspartate aminotransferase measurement | Alanine aminotransferase measurement
Item
ast/alt < 2 times uln
boolean
C0201899 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0201836 (UMLS CUI [2])
Exclusion Criteria | Pregnancy | Breast Feeding
Item
not pregnant or nursing
boolean
C0680251 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Fertility Contraceptive methods
Item
fertile patients must use effective contraception during and for 1 month after completion of study therapy
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
Exclusion | Medical condition Preventing Protocol Compliance
Item
no medical conditions that might prevent full participation in protocol-required testing or follow-up
boolean
C2828389 (UMLS CUI [1])
C3843040 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
C3843040 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
Exclusion Criteria | Institutionalized Persons | Prisoners
Item
no institutionalized patients (e.g., in prisons or mental health institutions)
boolean
C0680251 (UMLS CUI [1])
C0376326 (UMLS CUI [2])
C0033167 (UMLS CUI [3])
C0376326 (UMLS CUI [2])
C0033167 (UMLS CUI [3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Exclusion Criteria | Chemotherapy compromises Protocol Assessment | Therapeutic procedure compromises Protocol Assessment
Item
no concurrent chemotherapy or treatments that would compromise the safety and efficacy of protocol assessments
boolean
C0680251 (UMLS CUI [1])
C0392920 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C2348563 (UMLS CUI [2,3])
C1516048 (UMLS CUI [2,4])
C0087111 (UMLS CUI [3,1])
C2945640 (UMLS CUI [3,2])
C2348563 (UMLS CUI [3,3])
C1516048 (UMLS CUI [3,4])
C0392920 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C2348563 (UMLS CUI [2,3])
C1516048 (UMLS CUI [2,4])
C0087111 (UMLS CUI [3,1])
C2945640 (UMLS CUI [3,2])
C2348563 (UMLS CUI [3,3])
C1516048 (UMLS CUI [3,4])