ID

29325

Beskrivning

Use of the Combination of Olmesartan and Hydrochlorothiazide in Essential Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00430508

Länk

https://clinicaltrials.gov/show/NCT00430508

Nyckelord

Versioner (1)
  1. 2018-03-18 2018-03-18 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

18 mars 2018

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Essential Hypertension NCT00430508

Engelsk

Eligibility Essential Hypertension NCT00430508

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female europeans aged 18 years or older with moderate to severe hypertension (htn)
Beskrivning

European | Age | Hypertension, moderate | Hypertension, severe

Datatyp

boolean

Alias
UMLS CUI [1]
C0239307
UMLS CUI [2]
C0001779
UMLS CUI [3]
C1969581
UMLS CUI [4]
C4013784
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
female patients of childbearing potential pregnant, lactating or planning to become pregnant during the trial period.
Beskrivning

Childbearing Potential | Pregnancy | Breast Feeding | Pregnancy, Planned

Datatyp

boolean

Alias
UMLS CUI [1]
C3831118
UMLS CUI [2]
C0032961
UMLS CUI [3]
C0006147
UMLS CUI [4]
C0032992
patients with serious disorders which may limit the ability to evaluate the efficacy or safety of the study medication, including cerebrovascular, cardiovascular, renal, respiratory, hepatic, gastrointestinal, endocrine or metabolic, haematological or oncological, neurological and psychiatric diseases.
Beskrivning

Disease Serious | Evaluation Effectiveness Investigational New Drugs Limited | Evaluation Safety Investigational New Drugs Limited | Cerebrovascular Disorders | Cardiovascular Diseases | Kidney Diseases | Respiration Disorders | Liver diseases | Gastrointestinal Diseases | Endocrine System Diseases | Metabolic Diseases | Hematological Disease | Disease Oncologic | Nervous system disorder | Mental disorders

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205404
UMLS CUI [2,1]
C1261322
UMLS CUI [2,2]
C1280519
UMLS CUI [2,3]
C0013230
UMLS CUI [2,4]
C0439801
UMLS CUI [3,1]
C1261322
UMLS CUI [3,2]
C0036043
UMLS CUI [3,3]
C0013230
UMLS CUI [3,4]
C0439801
UMLS CUI [4]
C0007820
UMLS CUI [5]
C0007222
UMLS CUI [6]
C0022658
UMLS CUI [7]
C0035204
UMLS CUI [8]
C0023895
UMLS CUI [9]
C0017178
UMLS CUI [10]
C0014130
UMLS CUI [11]
C0025517
UMLS CUI [12]
C0018939
UMLS CUI [13,1]
C0012634
UMLS CUI [13,2]
C0205478
UMLS CUI [14]
C0027765
UMLS CUI [15]
C0004936
patients having a history of the following within the last six months:
Beskrivning

Medical History

Datatyp

boolean

Alias
UMLS CUI [1]
C0262926
myocardial infarction,
Beskrivning

Myocardial Infarction

Datatyp

boolean

Alias
UMLS CUI [1]
C0027051
unstable angina pectoris,
Beskrivning

Angina, Unstable

Datatyp

boolean

Alias
UMLS CUI [1]
C0002965
percutaneous coronary intervention,
Beskrivning

Percutaneous Coronary Intervention

Datatyp

boolean

Alias
UMLS CUI [1]
C1532338
severe heart failure,
Beskrivning

Heart failure Severe

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205082
hypertensive encephalopathy,
Beskrivning

Hypertensive Encephalopathy

Datatyp

boolean

Alias
UMLS CUI [1]
C0151620
cerebrovascular accident (stroke) or
Beskrivning

Cerebrovascular accident

Datatyp

boolean

Alias
UMLS CUI [1]
C0038454
transient ischaemic attack.
Beskrivning

Transient Ischemic Attack

Datatyp

boolean

Alias
UMLS CUI [1]
C0007787
patients with clinically significant abnormal laboratory values at screening.
Beskrivning

Laboratory test result abnormal

Datatyp

boolean

Alias
UMLS CUI [1]
C0438215
patients with secondary htn.
Beskrivning

Secondary hypertension

Datatyp

boolean

Alias
UMLS CUI [1]
C0155616
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Similar models

Eligibility Essential Hypertension NCT00430508

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
European | Age | Hypertension, moderate | Hypertension, severe
Item
male or female europeans aged 18 years or older with moderate to severe hypertension (htn)
boolean
C0239307 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C1969581 (UMLS CUI [3])
C4013784 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Childbearing Potential | Pregnancy | Breast Feeding | Pregnancy, Planned
Item
female patients of childbearing potential pregnant, lactating or planning to become pregnant during the trial period.
boolean
C3831118 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
C0032992 (UMLS CUI [4])
Disease Serious | Evaluation Effectiveness Investigational New Drugs Limited | Evaluation Safety Investigational New Drugs Limited | Cerebrovascular Disorders | Cardiovascular Diseases | Kidney Diseases | Respiration Disorders | Liver diseases | Gastrointestinal Diseases | Endocrine System Diseases | Metabolic Diseases | Hematological Disease | Disease Oncologic | Nervous system disorder | Mental disorders
Item
patients with serious disorders which may limit the ability to evaluate the efficacy or safety of the study medication, including cerebrovascular, cardiovascular, renal, respiratory, hepatic, gastrointestinal, endocrine or metabolic, haematological or oncological, neurological and psychiatric diseases.
boolean
C0012634 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C1261322 (UMLS CUI [2,1])
C1280519 (UMLS CUI [2,2])
C0013230 (UMLS CUI [2,3])
C0439801 (UMLS CUI [2,4])
C1261322 (UMLS CUI [3,1])
C0036043 (UMLS CUI [3,2])
C0013230 (UMLS CUI [3,3])
C0439801 (UMLS CUI [3,4])
C0007820 (UMLS CUI [4])
C0007222 (UMLS CUI [5])
C0022658 (UMLS CUI [6])
C0035204 (UMLS CUI [7])
C0023895 (UMLS CUI [8])
C0017178 (UMLS CUI [9])
C0014130 (UMLS CUI [10])
C0025517 (UMLS CUI [11])
C0018939 (UMLS CUI [12])
C0012634 (UMLS CUI [13,1])
C0205478 (UMLS CUI [13,2])
C0027765 (UMLS CUI [14])
C0004936 (UMLS CUI [15])
Medical History
Item
patients having a history of the following within the last six months:
boolean
C0262926 (UMLS CUI [1])
Myocardial Infarction
Item
myocardial infarction,
boolean
C0027051 (UMLS CUI [1])
Angina, Unstable
Item
unstable angina pectoris,
boolean
C0002965 (UMLS CUI [1])
Percutaneous Coronary Intervention
Item
percutaneous coronary intervention,
boolean
C1532338 (UMLS CUI [1])
Heart failure Severe
Item
severe heart failure,
boolean
C0018801 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Hypertensive Encephalopathy
Item
hypertensive encephalopathy,
boolean
C0151620 (UMLS CUI [1])
Cerebrovascular accident
Item
cerebrovascular accident (stroke) or
boolean
C0038454 (UMLS CUI [1])
Transient Ischemic Attack
Item
transient ischaemic attack.
boolean
C0007787 (UMLS CUI [1])
Laboratory test result abnormal
Item
patients with clinically significant abnormal laboratory values at screening.
boolean
C0438215 (UMLS CUI [1])
Secondary hypertension
Item
patients with secondary htn.
boolean
C0155616 (UMLS CUI [1])
Tillbaka till toppen 

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