Informações:
Falhas:
ID
28193
Descrição
Treatment Monitoring of Advanced Colorectal Cancer With 18F-FDG PET/CT; ODM derived from: https://clinicaltrials.gov/show/NCT00823810
Link
https://clinicaltrials.gov/show/NCT00823810
Palavras-chave
Versões (1)
- 28/12/2017 28/12/2017 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
28 de dezembro de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT00823810
Eligibility Colorectal Cancer NCT00823810
- StudyEvent: Eligibility
Similar models
Eligibility Colorectal Cancer NCT00823810
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Age
Item
age 40 to 80 years old
boolean
C0001779 (UMLS CUI [1])
Able to speak Finnish language | Able to speak Swedish language
Item
language spoken: finnish or swedish
boolean
C0564215 (UMLS CUI [1,1])
C0016134 (UMLS CUI [1,2])
C0564215 (UMLS CUI [2,1])
C0038996 (UMLS CUI [2,2])
C0016134 (UMLS CUI [1,2])
C0564215 (UMLS CUI [2,1])
C0038996 (UMLS CUI [2,2])
Karnofsky Performance Status | WHO performance status scale
Item
performance status: karnofsky score 70 or better or who performance status 2 or better
boolean
C0206065 (UMLS CUI [1])
C1298650 (UMLS CUI [2])
C1298650 (UMLS CUI [2])
Colorectal Carcinoma | Operative Surgical Procedures Neoplasm Metastasis
Item
earlier diagnosed (histologically confirmed) colorectal cancer with discovered metastases at operation
boolean
C0009402 (UMLS CUI [1])
C0543467 (UMLS CUI [2,1])
C0027627 (UMLS CUI [2,2])
C0543467 (UMLS CUI [2,1])
C0027627 (UMLS CUI [2,2])
Colorectal Carcinoma Treated | Clinical Study Follow-up | Colorectal cancer recurrent
Item
earlier diagnosed and treated colorectal cancer with discovered recurrence in the follow up
boolean
C0009402 (UMLS CUI [1,1])
C1522326 (UMLS CUI [1,2])
C3274571 (UMLS CUI [2])
C0854750 (UMLS CUI [3])
C1522326 (UMLS CUI [1,2])
C3274571 (UMLS CUI [2])
C0854750 (UMLS CUI [3])
Mental state | Comprehension Study Protocol
Item
mental status: patients must be able to understand the meaning of the study
boolean
C0278060 (UMLS CUI [1])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
Informed Consent
Item
informed consent: the patient must sign the appropriate ethical committee (ec) approved informed consent documents in the presence of the designated staff
boolean
C0021430 (UMLS CUI [1])
Cardiovascular Disease Serious | Liver disease Serious | Kidney Disease Serious
Item
prior medical history: patient must have no history of serious cardiovascular, liver or kidney disease
boolean
C0007222 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0022658 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
C0205404 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0022658 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
Study Subject At risk | Disabled Persons | Children | Pregnancy | Breast Feeding | Prisoners
Item
vulnerable study subjects such as described in finnish law concerning clinical studies (disabled, children, pregnant or breast-feeding women, prisoners) will not be included.
boolean
C0681850 (UMLS CUI [1,1])
C1444641 (UMLS CUI [1,2])
C0018576 (UMLS CUI [2])
C0008059 (UMLS CUI [3])
C0032961 (UMLS CUI [4])
C0006147 (UMLS CUI [5])
C0033167 (UMLS CUI [6])
C1444641 (UMLS CUI [1,2])
C0018576 (UMLS CUI [2])
C0008059 (UMLS CUI [3])
C0032961 (UMLS CUI [4])
C0006147 (UMLS CUI [5])
C0033167 (UMLS CUI [6])