ID

21965

Descrição

Two Cycles of PAD Combination by AHCT in MM; ODM derived from: https://clinicaltrials.gov/show/NCT01370434

Link

https://clinicaltrials.gov/show/NCT01370434

Palavras-chave

  1. 10/05/2017 10/05/2017 -
Transferido a

10 de maio de 2017

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Multiple Myeloma NCT01370434

Eligibility Multiple Myeloma NCT01370434

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
an active ms (attack or progression) during one month prior to inclusion or start of treatment.
Descrição

multiple sclerosis

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0026769
received treatment with glucocorticoids the last month prior to inclusion or start of treatment.
Descrição

glucocorticoids

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0017710
excessive fatigue or severe cognitive dysfunction related to ms that would preclude safe participation in the protocol.
Descrição

fatigue, cognitive dysfunction

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0015672
UMLS CUI [2]
C0338656
suffered from major depression or any other psychiatric disorder that would preclude safe participation in the protocol.
Descrição

psychiatric disorder, major depression

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0004936
UMLS CUI [2]
C1269683
heat intolerance.
Descrição

heat intolerance

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0231274
other serious concomitant disease that could preclude safe participation in the protocol.
Descrição

concomitant disease

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0243087
alcohol or drug abuse or consumption that could preclude participation according to the protocol and to attend the planned visits during the whole study period.
Descrição

alcohol or drug abuse

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0038586
breastfeeding or pregnancy
Descrição

pregnancy, breast feeding

Tipo de dados

boolean

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

Similar models

Eligibility Multiple Myeloma NCT01370434

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C0680251 (UMLS CUI)
multiple sclerosis
Item
an active ms (attack or progression) during one month prior to inclusion or start of treatment.
boolean
C0026769 (UMLS CUI [1])
glucocorticoids
Item
received treatment with glucocorticoids the last month prior to inclusion or start of treatment.
boolean
C0017710 (UMLS CUI [1])
fatigue, cognitive dysfunction
Item
excessive fatigue or severe cognitive dysfunction related to ms that would preclude safe participation in the protocol.
boolean
C0015672 (UMLS CUI [1])
C0338656 (UMLS CUI [2])
psychiatric disorder, major depression
Item
suffered from major depression or any other psychiatric disorder that would preclude safe participation in the protocol.
boolean
C0004936 (UMLS CUI [1])
C1269683 (UMLS CUI [2])
heat intolerance
Item
heat intolerance.
boolean
C0231274 (UMLS CUI [1])
concomitant disease
Item
other serious concomitant disease that could preclude safe participation in the protocol.
boolean
C0243087 (UMLS CUI [1])
alcohol or drug abuse
Item
alcohol or drug abuse or consumption that could preclude participation according to the protocol and to attend the planned visits during the whole study period.
boolean
C0038586 (UMLS CUI [1])
pregnancy, breast feeding
Item
breastfeeding or pregnancy
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])

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