Information:
Fel:
ID
18189
Beskrivning
A Multiple Myeloma Trial in Patients With Bone Metastases; ODM derived from: https://clinicaltrials.gov/show/NCT00104104
Länk
https://clinicaltrials.gov/show/NCT00104104
Nyckelord
Versioner (1)
- 2016-10-24 2016-10-24 -
Uppladdad den
24 oktober 2016
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Multiple Myeloma NCT00104104
Eligibility Multiple Myeloma NCT00104104
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Myeloma NCT00104104
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Age
Item
patients 18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Multiple Myeloma
Item
confirmed diagnosis of multiple myeloma
boolean
C0026764 (UMLS CUI [1])
Renal function Stable | Serum creatinine measurement Quantity
Item
stable renal function defined as two serum creatinine determinations of < 3 mg/dl
boolean
C0232804 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0201976 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0205360 (UMLS CUI [1,2])
C0201976 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
Estimation of creatinine clearance by Cockcroft-Gault formula
Item
calculated creatinine clearance of greater than or equal to 30 ml/min
boolean
C2711451 (UMLS CUI [1])
ECOG performance status
Item
ecog performance status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
Life Expectancy
Item
life expectancy of greater than or equal to 9 months
boolean
C0023671 (UMLS CUI [1])
Childbearing Potential Pregnancy test negative | Postmenopausal | Amenorrhea Duration
Item
if the patient is of child-bearing potential, a negative pregnancy test is required at screening, while postmenopausal women must be amenorrheic for at least 12 months to be considered of non-childbearing potential.
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
C0232970 (UMLS CUI [2])
C0002453 (UMLS CUI [3,1])
C0449238 (UMLS CUI [3,2])
C0427780 (UMLS CUI [1,2])
C0232970 (UMLS CUI [2])
C0002453 (UMLS CUI [3,1])
C0449238 (UMLS CUI [3,2])
Protocol Compliance | Informed Consent
Item
ability to comply with trial requirements and give informed consent.
boolean
C0525058 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
C0021430 (UMLS CUI [2])
Diphosphonates Intravenous
Item
iv bisphosphonate therapy for more than 3 years.
boolean
C0012544 (UMLS CUI [1,1])
C1522726 (UMLS CUI [1,2])
C1522726 (UMLS CUI [1,2])
amyloidosis
Item
patients with a diagnosis of amyloidosis.
boolean
C0002726 (UMLS CUI [1])
Hypersensitivity zoledronic acid | Hypersensitivity Diphosphonates
Item
known hypersensitivity to zoledronic acid or other bisphosphonates
boolean
C0020517 (UMLS CUI [1,1])
C0257685 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0012544 (UMLS CUI [2,2])
C0257685 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0012544 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant patients or lactating patients.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Childbearing Potential Contraceptive methods
Item
women of childbearing potential not on a medically recognized form of contraception
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
Cardiovascular Disease Uncontrolled | Uncontrolled hypertension | DIABETES MELLITUS NON INSULIN DEPENDENT UNCONTROLLED
Item
patients with uncontrolled cardiovascular disease, hypertension, and type 2 diabetes mellitus.
boolean
C0007222 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C1868885 (UMLS CUI [2])
C0743118 (UMLS CUI [3])
C0205318 (UMLS CUI [1,2])
C1868885 (UMLS CUI [2])
C0743118 (UMLS CUI [3])