Information:
Fel:
ID
21846
Beskrivning
Combination Chemotherapy of Gemcitabine and Paclitaxel for Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00334802
Länk
https://clinicaltrials.gov/show/NCT00334802
Nyckelord
Versioner (1)
- 2017-05-03 2017-05-03 -
Uppladdad den
3 maj 2017
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Metastatic Breast Cancer NCT00334802
Eligibility Metastatic Breast Cancer NCT00334802
- StudyEvent: Eligibility
Similar models
Eligibility Metastatic Breast Cancer NCT00334802
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Breast Carcinoma
Item
histologically and/or cytologically confirmed breast cancer
boolean
C0678222 (UMLS CUI [1])
Adjuvant Chemotherapy Breast Carcinoma | Neoadjuvant Chemotherapy Breast Carcinoma | Anthracycline
Item
received adjuvant/neo-adjuvant chemotherapy for breast cancer with anthracycline regimen
boolean
C0085533 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0600558 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
C0678222 (UMLS CUI [2,3])
C0003234 (UMLS CUI [3])
C0678222 (UMLS CUI [1,2])
C0600558 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
C0678222 (UMLS CUI [2,3])
C0003234 (UMLS CUI [3])
Region Measurable Quantity
Item
to have at least one measurable region
boolean
C0205147 (UMLS CUI [1,1])
C1513040 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1513040 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance status: 0-1
boolean
C1520224 (UMLS CUI [1])
Organ function | Bone Marrow function | Liver function | Renal function
Item
to have adequate organ function (bone marrow, liver and renal function)
boolean
C0678852 (UMLS CUI [1])
C0005953 (UMLS CUI [2,1])
C0031843 (UMLS CUI [2,2])
C0232741 (UMLS CUI [3])
C0232804 (UMLS CUI [4])
C0005953 (UMLS CUI [2,1])
C0031843 (UMLS CUI [2,2])
C0232741 (UMLS CUI [3])
C0232804 (UMLS CUI [4])
Pneumonia, Interstitial | Pulmonary Fibrosis
Item
to have interstitial pneumonia or pulmonary fibrosis
boolean
C0206061 (UMLS CUI [1])
C0034069 (UMLS CUI [2])
C0034069 (UMLS CUI [2])
Inflammatory Breast Carcinoma
Item
to have inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1])
Chemotherapy | Therapeutic radiology procedure | Hormone Therapy | Immunotherapy | Operative Surgical Procedures
Item
within 28 days after the latest chemotherapy or radiotherapy, 14 days after the latest hormonal/immunotherapy or 7 days after surgery
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C0279025 (UMLS CUI [3])
C0021083 (UMLS CUI [4])
C0543467 (UMLS CUI [5])
C1522449 (UMLS CUI [2])
C0279025 (UMLS CUI [3])
C0021083 (UMLS CUI [4])
C0543467 (UMLS CUI [5])
Metastatic malignant neoplasm to brain Symptoms
Item
to have brain metastases with symptoms
boolean
C0220650 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,2])
Severe medical complication | Myocardial Infarction | Communicable Disease | Drug Allergy | Diabetes Mellitus
Item
to have severe complication (cardiac infarction, infection, drug hypersensitivity or diabetes)
boolean
C3495031 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0009450 (UMLS CUI [3])
C0013182 (UMLS CUI [4])
C0011849 (UMLS CUI [5])
C0027051 (UMLS CUI [2])
C0009450 (UMLS CUI [3])
C0013182 (UMLS CUI [4])
C0011849 (UMLS CUI [5])