ID
37017
Beschreibung
Management Of The Infusion-Associated Reactions In RRMS Patients Treated With LEMTRADA; ODM derived from: https://clinicaltrials.gov/show/NCT02205489
Link
https://clinicaltrials.gov/show/NCT02205489
Stichworte
Versionen (1)
- 30.06.19 30.06.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
30. Juni 2019
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Relapsing-remitting Multiple Sclerosis NCT02205489
Eligibility Relapsing-remitting Multiple Sclerosis NCT02205489
- StudyEvent: Eligibility
Beschreibung
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschreibung
Prior Therapy Lemtrada
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1514463
- UMLS CUI [1,2]
- C3860145
Beschreibung
Medical contraindication Lemtrada
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C3860145
Beschreibung
Medical contraindication Therapy Symptomatic
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C0087111
- UMLS CUI [1,3]
- C0231220
Beschreibung
Study Subject Participation Status | Interventional Study Investigational
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2,1]
- C3274035
- UMLS CUI [2,2]
- C1517586
Beschreibung
Technical Problem Study Subject Participation Status Excluded | Factor Administrative Study Subject Participation Status Excluded
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1710348
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0332196
- UMLS CUI [2,1]
- C1521761
- UMLS CUI [2,2]
- C3845829
- UMLS CUI [2,3]
- C2348568
- UMLS CUI [2,4]
- C0332196
Beschreibung
Persons Involved Completion of clinical trial | Research Personnel | Research Personnel Relative
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0027361
- UMLS CUI [1,2]
- C1314939
- UMLS CUI [1,3]
- C2732579
- UMLS CUI [2]
- C0035173
- UMLS CUI [3,1]
- C0035173
- UMLS CUI [3,2]
- C0080103
Beschreibung
Consent Withdrawn
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1707492
Beschreibung
Enrollment Discontinued
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1516879
- UMLS CUI [1,2]
- C1444662
Beschreibung
Childbearing Potential Contraceptive methods Absent | Childbearing Potential Pregnancy Test Unwilling | Childbearing Potential Pregnancy Test Unable
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C3831118
- UMLS CUI [1,2]
- C0700589
- UMLS CUI [1,3]
- C0332197
- UMLS CUI [2,1]
- C3831118
- UMLS CUI [2,2]
- C0032976
- UMLS CUI [2,3]
- C0558080
- UMLS CUI [3,1]
- C3831118
- UMLS CUI [3,2]
- C0032976
- UMLS CUI [3,3]
- C1299582
Beschreibung
Pregnancy | Hematologic Test Beta HCG positive | Breast Feeding
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2,1]
- C0018941
- UMLS CUI [2,2]
- C0813152
- UMLS CUI [3]
- C0006147
Beschreibung
Latent Tuberculosis | Tuberculosis
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1609538
- UMLS CUI [2]
- C0041296
Beschreibung
Hepatitis B | Hepatitis C
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0019163
- UMLS CUI [2]
- C0019196
Beschreibung
Study Subject Participation Status | Considerations Additional
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2,1]
- C0518609
- UMLS CUI [2,2]
- C1524062
Ähnliche Modelle
Eligibility Relapsing-remitting Multiple Sclerosis NCT02205489
- StudyEvent: Eligibility
C0001675 (UMLS CUI [2])
C1301880 (UMLS CUI [3,1])
C3860145 (UMLS CUI [3,2])
C3860145 (UMLS CUI [1,2])
C3860145 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C0231220 (UMLS CUI [1,3])
C3274035 (UMLS CUI [2,1])
C1517586 (UMLS CUI [2,2])
C2348568 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])
C1521761 (UMLS CUI [2,1])
C3845829 (UMLS CUI [2,2])
C2348568 (UMLS CUI [2,3])
C0332196 (UMLS CUI [2,4])
C1314939 (UMLS CUI [1,2])
C2732579 (UMLS CUI [1,3])
C0035173 (UMLS CUI [2])
C0035173 (UMLS CUI [3,1])
C0080103 (UMLS CUI [3,2])
C1444662 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C3831118 (UMLS CUI [2,1])
C0032976 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
C3831118 (UMLS CUI [3,1])
C0032976 (UMLS CUI [3,2])
C1299582 (UMLS CUI [3,3])
C0018941 (UMLS CUI [2,1])
C0813152 (UMLS CUI [2,2])
C0006147 (UMLS CUI [3])
C0041296 (UMLS CUI [2])
C0019196 (UMLS CUI [2])
C0518609 (UMLS CUI [2,1])
C1524062 (UMLS CUI [2,2])