ID

22393

Description

Comparison of Bone Effects With Copaxone and Interferon in Multiple Sclerosis; ODM derived from: https://clinicaltrials.gov/show/NCT00490906

Link

https://clinicaltrials.gov/show/NCT00490906

Keywords

  1. 6/1/17 6/1/17 -
Uploaded on

June 1, 2017

DOI

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License

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT00490906

Eligibility Multiple Sclerosis NCT00490906

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female, age > 18
Description

gender, age

Data type

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0001779
able to understand and give informed consent
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
relapsing remitting multiple sclerosis (rrms)
Description

rrms

Data type

boolean

Alias
UMLS CUI [1]
C0751967
treatment with interferons or copaxone for at least one year prior to study entry
Description

beta interferon therapy, copaxone

Data type

boolean

Alias
UMLS CUI [1]
C0854622
UMLS CUI [2]
C0528175
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known osteoporosis
Description

osteoporosis

Data type

boolean

Alias
UMLS CUI [1]
C0029456
history of hypercalcemia
Description

history of hypercalcemia

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0020437
currently pregnant
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
history of primary hyperparathyroidism, hyperthyroidism, or hypothyroidism
Description

history of primary hyperparathyroidism, hyperthyroidism, or hypothyroidism

Data type

boolean

Alias
UMLS CUI [1]
C0221002
UMLS CUI [2]
C0020550
UMLS CUI [3]
C0020676
unstable medical condition
Description

unstable medical condition

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0443343
ongoing use of bisphosphonates
Description

bisphosphonates

Data type

boolean

Alias
UMLS CUI [1]
C0012544

Similar models

Eligibility Multiple Sclerosis NCT00490906

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
gender, age
Item
female, age > 18
boolean
C0079399 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
informed consent
Item
able to understand and give informed consent
boolean
C0021430 (UMLS CUI [1])
rrms
Item
relapsing remitting multiple sclerosis (rrms)
boolean
C0751967 (UMLS CUI [1])
beta interferon therapy, copaxone
Item
treatment with interferons or copaxone for at least one year prior to study entry
boolean
C0854622 (UMLS CUI [1])
C0528175 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
osteoporosis
Item
known osteoporosis
boolean
C0029456 (UMLS CUI [1])
history of hypercalcemia
Item
history of hypercalcemia
boolean
C0262926 (UMLS CUI [1,1])
C0020437 (UMLS CUI [1,2])
pregnancy
Item
currently pregnant
boolean
C0032961 (UMLS CUI [1])
history of primary hyperparathyroidism, hyperthyroidism, or hypothyroidism
Item
history of primary hyperparathyroidism, hyperthyroidism, or hypothyroidism
boolean
C0221002 (UMLS CUI [1])
C0020550 (UMLS CUI [2])
C0020676 (UMLS CUI [3])
unstable medical condition
Item
unstable medical condition
boolean
C0012634 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
bisphosphonates
Item
ongoing use of bisphosphonates
boolean
C0012544 (UMLS CUI [1])

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