ID

23814

Beschrijving

A Study of Bevacizumab (Avastin) in Combination With Capecitabine (Xeloda) in Elderly Patients With Metastatic Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00484939

Link

https://clinicaltrials.gov/show/NCT00484939

Trefwoorden

  1. 14-07-17 14-07-17 -
Geüploaded op

14 juli 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Colorectal Cancer NCT00484939

Eligibility Colorectal Cancer NCT00484939

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, ≥ 70 years of age.
Beschrijving

Adult | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0001779
cancer of the colon or rectum.
Beschrijving

Colon Carcinoma | Rectal Carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0699790
UMLS CUI [2]
C0007113
metastatic disease diagnosed ≤ 6 months before enrollment.
Beschrijving

Neoplasm Metastasis

Datatype

boolean

Alias
UMLS CUI [1]
C0027627
≥ 1 measurable metastatic lesion.
Beschrijving

Metastatic Lesion Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C1513183
UMLS CUI [1,2]
C1265611
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
adjuvant anti-vascular endothelial growth factor (vegf) treatment.
Beschrijving

VEGFR Inhibitor Adjuvant

Datatype

boolean

Alias
UMLS CUI [1,1]
C2985521
UMLS CUI [1,2]
C1522673
prior chemotherapeutic treatment for metastatic colorectal cancer.
Beschrijving

Chemotherapy Colorectal cancer metastatic

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0948380
past or current history of other malignancies (with the exception of basal and squamous cell cancer of the skin, or in situ cancer of the cervix).
Beschrijving

Malignant Neoplasms | Basal cell carcinoma | Squamous cell carcinoma of skin | Carcinoma in situ of uterine cervix

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0007117
UMLS CUI [3]
C0553723
UMLS CUI [4]
C0851140
clinically significant cardiovascular disease.
Beschrijving

Cardiovascular Diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0007222
current or recent daily use of aspirin (> 325 mg/day) or other non-steroidal anti-inflammatory drug (nsaid), or full dose anticoagulants.
Beschrijving

Aspirin U/day | Anti-Inflammatory Agents, Non-Steroidal | Anticoagulants Dose Full

Datatype

boolean

Alias
UMLS CUI [1,1]
C0004057
UMLS CUI [1,2]
C0456683
UMLS CUI [2]
C0003211
UMLS CUI [3,1]
C0003280
UMLS CUI [3,2]
C0178602
UMLS CUI [3,3]
C0443225

Similar models

Eligibility Colorectal Cancer NCT00484939

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Age
Item
adult patients, ≥ 70 years of age.
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Colon Carcinoma | Rectal Carcinoma
Item
cancer of the colon or rectum.
boolean
C0699790 (UMLS CUI [1])
C0007113 (UMLS CUI [2])
Neoplasm Metastasis
Item
metastatic disease diagnosed ≤ 6 months before enrollment.
boolean
C0027627 (UMLS CUI [1])
Metastatic Lesion Quantity
Item
≥ 1 measurable metastatic lesion.
boolean
C1513183 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
VEGFR Inhibitor Adjuvant
Item
adjuvant anti-vascular endothelial growth factor (vegf) treatment.
boolean
C2985521 (UMLS CUI [1,1])
C1522673 (UMLS CUI [1,2])
Chemotherapy Colorectal cancer metastatic
Item
prior chemotherapeutic treatment for metastatic colorectal cancer.
boolean
C0392920 (UMLS CUI [1,1])
C0948380 (UMLS CUI [1,2])
Malignant Neoplasms | Basal cell carcinoma | Squamous cell carcinoma of skin | Carcinoma in situ of uterine cervix
Item
past or current history of other malignancies (with the exception of basal and squamous cell cancer of the skin, or in situ cancer of the cervix).
boolean
C0006826 (UMLS CUI [1])
C0007117 (UMLS CUI [2])
C0553723 (UMLS CUI [3])
C0851140 (UMLS CUI [4])
Cardiovascular Diseases
Item
clinically significant cardiovascular disease.
boolean
C0007222 (UMLS CUI [1])
Aspirin U/day | Anti-Inflammatory Agents, Non-Steroidal | Anticoagulants Dose Full
Item
current or recent daily use of aspirin (> 325 mg/day) or other non-steroidal anti-inflammatory drug (nsaid), or full dose anticoagulants.
boolean
C0004057 (UMLS CUI [1,1])
C0456683 (UMLS CUI [1,2])
C0003211 (UMLS CUI [2])
C0003280 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0443225 (UMLS CUI [3,3])

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