Informatie:
Fout:
ID
24624
Beschrijving
Chemotherapy and Avastin Followed by Maintenance Treatment With Avastin +/- Tarceva; ODM derived from: https://clinicaltrials.gov/show/NCT00598156
Link
https://clinicaltrials.gov/show/NCT00598156
Trefwoorden
Versies (1)
- 09-08-17 09-08-17 -
Geüploaded op
9 augustus 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Metastatic Colorectal Cancer NCT00598156
Eligibility Metastatic Colorectal Cancer NCT00598156
- StudyEvent: Eligibility
Similar models
Eligibility Metastatic Colorectal Cancer NCT00598156
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Adenocarcinoma of colon | Adenocarcinoma of rectum
Item
1. adenocarcinoma of the colon or rectum.
boolean
C0338106 (UMLS CUI [1])
C0149978 (UMLS CUI [2])
C0149978 (UMLS CUI [2])
Age
Item
2. age > 18.
boolean
C0001779 (UMLS CUI [1])
Measurable Disease
Item
3. measurable disease according to recist criteria.
boolean
C1513041 (UMLS CUI [1])
Life Expectancy
Item
4. expected survival more than three months.
boolean
C0023671 (UMLS CUI [1])
Bone Marrow function | Liver function | Renal function
Item
5. adequate bone marrow, liver and kidney function.
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
International Normalized Ratio
Item
6. inr < 1.5 times upper limit.
boolean
C0525032 (UMLS CUI [1])
Fertility Contraceptive methods
Item
7. adequate contraception for fertile patients.
boolean
C0015895 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
Informed Consent
Item
8. signed written informed consent.
boolean
C0021430 (UMLS CUI [1])
Chemotherapy Colorectal cancer metastatic
Item
1. earlier chemotherapy for metastatic colorectal cancer.
boolean
C0392920 (UMLS CUI [1,1])
C0948380 (UMLS CUI [1,2])
C0948380 (UMLS CUI [1,2])
Adjuvant therapy
Item
2. adjuvant treatment within 6 months.
boolean
C0677850 (UMLS CUI [1])
Operative Surgical Procedures | Trauma
Item
3. surgery or significant trauma within 28 days prior to study entry.
boolean
C0543467 (UMLS CUI [1])
C3714660 (UMLS CUI [2])
C3714660 (UMLS CUI [2])
Therapeutic radiology procedure Planned Target Lesion
Item
4. planned radiotherapy against target lesions.
boolean
C1522449 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1521840 (UMLS CUI [1,3])
C0221198 (UMLS CUI [1,4])
C1301732 (UMLS CUI [1,2])
C1521840 (UMLS CUI [1,3])
C0221198 (UMLS CUI [1,4])
CNS metastases
Item
5. cns metastases.
boolean
C0686377 (UMLS CUI [1])
Malignant Neoplasms | Exception Carcinoma in situ of uterine cervix | Exception Basal cell carcinoma
Item
6. prior malignancy within 5 years except ca in situ of cervix and basal cell carcinoma.
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0851140 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0007117 (UMLS CUI [3,2])
C1705847 (UMLS CUI [2,1])
C0851140 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0007117 (UMLS CUI [3,2])
Bleeding tendency
Item
7. bleeding diathesis
boolean
C1458140 (UMLS CUI [1])
Uncontrolled hypertension
Item
8. uncontrolled hypertension.
boolean
C1868885 (UMLS CUI [1])
Cardiovascular Disease
Item
9. significant cardiovascular disease.
boolean
C0007222 (UMLS CUI [1])
Anticoagulants
Item
10. treatment with anticoagulant drugs.
boolean
C0003280 (UMLS CUI [1])
Study Subject Participation Status
Item
11. participation in other clinical trial.
boolean
C2348568 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
12. pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])