ID

30866

Beschrijving

Pharmacokinetics of Lenalidomide (Revlimid®) in Patients With Multiple Myeloma and Impaired Renal Function; ODM derived from: https://clinicaltrials.gov/show/NCT00779922

Link

https://clinicaltrials.gov/show/NCT00779922

Trefwoorden

  1. 28-06-18 28-06-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

28 juni 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Multiple Myeloma NCT00779922

Eligibility Multiple Myeloma NCT00779922

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
documented diagnosis of relapsed or refractory multiple myeloma (mm).
Beschrijving

Recurrent multiple myeloma | Refractory multiple myeloma

Datatype

boolean

Alias
UMLS CUI [1]
C1370446
UMLS CUI [2]
C0278620
age > 18 years at the time of signing the informed consent form
Beschrijving

Age | Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0021430
stable renal function
Beschrijving

Renal function Stable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0232804
UMLS CUI [1,2]
C0205360
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
documented amyloidosis
Beschrijving

Amyloidosis

Datatype

boolean

Alias
UMLS CUI [1]
C0002726
any prior use of revlimid ®
Beschrijving

Revlimid

Datatype

boolean

Alias
UMLS CUI [1]
C1135145
any contraindication to revlimid ® and especially:
Beschrijving

Medical contraindication Revlimid

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1135145
lack of acceptable method of birth control for female of childbearing potential (fcpb)
Beschrijving

Childbearing Potential Contraceptive methods Lacking

Datatype

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0332268
men who don't agree to use condom during the study and 4 weeks after the last study drug intake if their partner is a fcpb.
Beschrijving

Gender Male Condoms Unwilling | Partner Childbearing Potential

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0009653
UMLS CUI [1,3]
C0558080
UMLS CUI [2,1]
C0682323
UMLS CUI [2,2]
C3831118
pregnant or breast feeding women
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147

Similar models

Eligibility Multiple Myeloma NCT00779922

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Recurrent multiple myeloma | Refractory multiple myeloma
Item
documented diagnosis of relapsed or refractory multiple myeloma (mm).
boolean
C1370446 (UMLS CUI [1])
C0278620 (UMLS CUI [2])
Age | Informed Consent
Item
age > 18 years at the time of signing the informed consent form
boolean
C0001779 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
Renal function Stable
Item
stable renal function
boolean
C0232804 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Amyloidosis
Item
documented amyloidosis
boolean
C0002726 (UMLS CUI [1])
Revlimid
Item
any prior use of revlimid ®
boolean
C1135145 (UMLS CUI [1])
Medical contraindication Revlimid
Item
any contraindication to revlimid ® and especially:
boolean
C1301624 (UMLS CUI [1,1])
C1135145 (UMLS CUI [1,2])
Childbearing Potential Contraceptive methods Lacking
Item
lack of acceptable method of birth control for female of childbearing potential (fcpb)
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Gender Male Condoms Unwilling | Partner Childbearing Potential
Item
men who don't agree to use condom during the study and 4 weeks after the last study drug intake if their partner is a fcpb.
boolean
C0079399 (UMLS CUI [1,1])
C0009653 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0682323 (UMLS CUI [2,1])
C3831118 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant or breast feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])

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