ID

13065

Description

Dexamethasone or Dexamethasone in Combination With Thalidomide as Salvage Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT00083902

Link

https://clinicaltrials.gov/show/NCT00083902

Keywords

  1. 1/14/16 1/14/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 14, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Multiple Myeloma NCT00083902

Eligibility Multiple Myeloma NCT00083902

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients must have a confirmed diagnosis of previously treated, active multiple myeloma, with hypoproliferative/low risk relapse following at least one autologous transplant.
Description

multiple myeloma

Data type

boolean

Alias
UMLS CUI [1]
C0026764
UMLS CUI [2]
C0194037
patients must be 18 years of age or older. women of childbearing age and fertile men must use a medically acceptable means of birth control while on study and for 6 months thereafter.
Description

age, contraception

Data type

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0700589
patients must sign an informed consent to participate in this study, and be fully aware of the known teratogenic potential of this drug combination.
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
patients must have a swog performance status of 0-2.
Description

performance status

Data type

boolean

Alias
UMLS CUI [1]
C1518965
patients must have adequate renal function, as defined by serum creatinine < or = 3.0 mg/dl.
Description

renal function

Data type

boolean

Alias
UMLS CUI [1]
C0201976
patients must be off chemotherapy (including steroids) and local radiotherapy for > or equal 3 weeks prior to entering the study.
Description

chemotherapy, radiotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
no other concurrent therapy for myeloma is permitted while on protocol.
Description

no other concurrent therapy

Data type

boolean

Alias
UMLS CUI [1]
C0087111
there must be no evidence of active infection requiring iv antibiotics.
Description

active infection

Data type

boolean

Alias
UMLS CUI [1]
C0009450

Similar models

Eligibility Multiple Myeloma NCT00083902

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
multiple myeloma
Item
all patients must have a confirmed diagnosis of previously treated, active multiple myeloma, with hypoproliferative/low risk relapse following at least one autologous transplant.
boolean
C0026764 (UMLS CUI [1])
C0194037 (UMLS CUI [2])
age, contraception
Item
patients must be 18 years of age or older. women of childbearing age and fertile men must use a medically acceptable means of birth control while on study and for 6 months thereafter.
boolean
C0001779 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
informed consent
Item
patients must sign an informed consent to participate in this study, and be fully aware of the known teratogenic potential of this drug combination.
boolean
C0021430 (UMLS CUI [1])
performance status
Item
patients must have a swog performance status of 0-2.
boolean
C1518965 (UMLS CUI [1])
renal function
Item
patients must have adequate renal function, as defined by serum creatinine < or = 3.0 mg/dl.
boolean
C0201976 (UMLS CUI [1])
chemotherapy, radiotherapy
Item
patients must be off chemotherapy (including steroids) and local radiotherapy for > or equal 3 weeks prior to entering the study.
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
no other concurrent therapy
Item
no other concurrent therapy for myeloma is permitted while on protocol.
boolean
C0087111 (UMLS CUI [1])
active infection
Item
there must be no evidence of active infection requiring iv antibiotics.
boolean
C0009450 (UMLS CUI [1])

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