ID
26005
Description
A Study to Assess the Safety, Tolerability and Efficacy of RG2417 in Bipolar I Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00812058
Link
https://clinicaltrials.gov/show/NCT00812058
Keywords
Versions (2)
- 10/2/17 10/2/17 -
- 10/4/17 10/4/17 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
October 4, 2017
DOI
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License
Creative Commons BY 4.0
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Eligibility Bipolar I Depression NCT00812058
Eligibility Bipolar I Depression NCT00812058
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Manic episode | Hypomanic episode | Mixed bipolar I disorder
Data type
boolean
Alias
- UMLS CUI [1]
- C0349208
- UMLS CUI [2]
- C1396834
- UMLS CUI [3]
- C0236780
Description
Rapid cycling bipolar I disorder | Mood Episode Quantity
Data type
boolean
Alias
- UMLS CUI [1]
- C2063820
- UMLS CUI [2,1]
- C0026516
- UMLS CUI [2,2]
- C0332189
- UMLS CUI [2,3]
- C1265611
Description
Dementia Treatment required for | Axis I diagnosis Treatment required for | Exception Bipolar I disorder
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0497327
- UMLS CUI [1,2]
- C0332121
- UMLS CUI [2,1]
- C0270287
- UMLS CUI [2,2]
- C0332121
- UMLS CUI [3,1]
- C1705847
- UMLS CUI [3,2]
- C0853193
Description
Substance Dependence | Substance Use Disorders
Data type
boolean
Alias
- UMLS CUI [1]
- C0038580
- UMLS CUI [2]
- C0038586
Description
Urine drug screen positive Amphetamines | Urine drug screen positive Cocaine metabolite | Urine drug screen positive Opiates | Urine drug screen positive Phencyclidine
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0743300
- UMLS CUI [1,2]
- C0002667
- UMLS CUI [2,1]
- C0743300
- UMLS CUI [2,2]
- C1455816
- UMLS CUI [3,1]
- C0743300
- UMLS CUI [3,2]
- C0376196
- UMLS CUI [4,1]
- C0743300
- UMLS CUI [4,2]
- C0031381
Description
Axis II diagnosis Interferes with Protocol Compliance
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0270288
- UMLS CUI [1,2]
- C0521102
- UMLS CUI [1,3]
- C0525058
Description
At risk for suicide Serious | Homicide At risk Serious
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0563664
- UMLS CUI [1,2]
- C0205404
- UMLS CUI [2,1]
- C0019872
- UMLS CUI [2,2]
- C1444641
- UMLS CUI [2,3]
- C0205404
Description
Hypersensitivity Investigational New Drug Ingredient | ALLERGY TO LACTOSE
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C1550600
- UMLS CUI [2]
- C0744078
Description
Pregnancy | Breast Feeding | Gender Contraceptive methods Refused
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
- UMLS CUI [3,1]
- C0079399
- UMLS CUI [3,2]
- C0700589
- UMLS CUI [3,3]
- C1705116
Description
Epilepsy
Data type
boolean
Alias
- UMLS CUI [1]
- C0014544
Description
Depressive disorder Episode Duration
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0011581
- UMLS CUI [1,2]
- C0332189
- UMLS CUI [1,3]
- C0449238
Similar models
Eligibility Bipolar I Depression NCT00812058
- StudyEvent: Eligibility
C1265611 (UMLS CUI [1,2])
C0236780 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C1514873 (UMLS CUI [3,1])
C0013216 (UMLS CUI [3,2])
C0746402 (UMLS CUI [3,3])
C1396834 (UMLS CUI [2])
C0236780 (UMLS CUI [3])
C0026516 (UMLS CUI [2,1])
C0332189 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0332121 (UMLS CUI [1,2])
C0270287 (UMLS CUI [2,1])
C0332121 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0853193 (UMLS CUI [3,2])
C0038586 (UMLS CUI [2])
C0002667 (UMLS CUI [1,2])
C0743300 (UMLS CUI [2,1])
C1455816 (UMLS CUI [2,2])
C0743300 (UMLS CUI [3,1])
C0376196 (UMLS CUI [3,2])
C0743300 (UMLS CUI [4,1])
C0031381 (UMLS CUI [4,2])
C0521102 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0205404 (UMLS CUI [1,2])
C0019872 (UMLS CUI [2,1])
C1444641 (UMLS CUI [2,2])
C0205404 (UMLS CUI [2,3])
C0013230 (UMLS CUI [1,2])
C1550600 (UMLS CUI [1,3])
C0744078 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C1705116 (UMLS CUI [3,3])
C0332189 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])