ID

17378

Descrição

Olmesartan Medoxomil in Hypertension and Renal Impairment; ODM derived from: https://clinicaltrials.gov/show/NCT00151827

Link

https://clinicaltrials.gov/show/NCT00151827

Palavras-chave

Versões (1)
  1. 10/09/2016 10/09/2016 -
Transferido a

10 de setembro de 2016

DOI

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Licença

Creative Commons BY 4.0
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Eligibility Essential Hypertension NCT00151827

Inglês

Eligibility Essential Hypertension NCT00151827

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
mean sitting bp prior to randomization of 140-180/90-109 mmhg;
Descrição

Sitting blood pressure mean

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0580946
UMLS CUI [1,2]
C0444504
renal impairment prior to randomization of mild (50 ≤ clcr ≥ 80 ml/min) to moderate (30 ≤ clcr ≥50 ml/min) severity
Descrição

Renal Insufficiency Mild | Renal Insufficiency Moderate | Creatinine clearance measurement

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C2945599
UMLS CUI [2,1]
C1565489
UMLS CUI [2,2]
C0205081
UMLS CUI [3]
C0373595
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
malignant hypertension or sitting bp greater than 180/109 mmhg;
Descrição

Malignant Hypertension | Sitting blood pressure

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0020540
UMLS CUI [2]
C0580946
severe heart failure, severe renal disease;
Descrição

Heart failure Severe | Kidney Disease Severe

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0022658
UMLS CUI [2,2]
C0205082
recent history of myocardial infarction, stroke or transient ischemic attack;
Descrição

Myocardial Infarction | Cerebrovascular accident | Transient Ischemic Attack

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0007787
history, clinical or current evidence of any significant gastrointestinal, respiratory, hematological, metabolic, immunological or any other underlying disease which in the opinion of the investigator would interfere with the patient's participation in the trial;
Descrição

Gastrointestinal Disease Significant Evidence of | Respiration Disorder | Hematological Disease | Metabolic Disease | Immune System Disease | Disease Interferes with Study Subject Participation Status

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0017178
UMLS CUI [1,2]
C0750502
UMLS CUI [1,3]
C0332120
UMLS CUI [2]
C0035204
UMLS CUI [3]
C0018939
UMLS CUI [4]
C0025517
UMLS CUI [5]
C0021053
UMLS CUI [6,1]
C0012634
UMLS CUI [6,2]
C0521102
UMLS CUI [6,3]
C2348568
hypersensitivity or contraindications to arbs or ace inhibitors or any cross allergy;
Descrição

Hypersensitivity Angiotensin II receptor antagonist | Medical contraindication Angiotensin II receptor antagonist | Hypersensitivity Angiotensin-Converting Enzyme Inhibitors | Medical contraindication Angiotensin-Converting Enzyme Inhibitors | Hypersensitivity Allergens Cross Reactive

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0521942
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0521942
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C0003015
UMLS CUI [4,1]
C1301624
UMLS CUI [4,2]
C0003015
UMLS CUI [5,1]
C0020517
UMLS CUI [5,2]
C0002092
UMLS CUI [5,3]
C0010357
treatment with dis-allowed medication;
Descrição

Illicit Drugs

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0086190
pregnant or breastfeeding females or females of childbearing potential without adequate contraception;
Descrição

Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Inadequate

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0700589
UMLS CUI [3,3]
C0205412
history of drug and/or alcohol abuse
Descrição

Substance Use Disorders

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0038586
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Similar models

Eligibility Essential Hypertension NCT00151827

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Sitting blood pressure mean
Item
mean sitting bp prior to randomization of 140-180/90-109 mmhg;
boolean
C0580946 (UMLS CUI [1,1])
C0444504 (UMLS CUI [1,2])
Renal Insufficiency Mild | Renal Insufficiency Moderate | Creatinine clearance measurement
Item
renal impairment prior to randomization of mild (50 ≤ clcr ≥ 80 ml/min) to moderate (30 ≤ clcr ≥50 ml/min) severity
boolean
C1565489 (UMLS CUI [1,1])
C2945599 (UMLS CUI [1,2])
C1565489 (UMLS CUI [2,1])
C0205081 (UMLS CUI [2,2])
C0373595 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Malignant Hypertension | Sitting blood pressure
Item
malignant hypertension or sitting bp greater than 180/109 mmhg;
boolean
C0020540 (UMLS CUI [1])
C0580946 (UMLS CUI [2])
Heart failure Severe | Kidney Disease Severe
Item
severe heart failure, severe renal disease;
boolean
C0018801 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0022658 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Myocardial Infarction | Cerebrovascular accident | Transient Ischemic Attack
Item
recent history of myocardial infarction, stroke or transient ischemic attack;
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
Gastrointestinal Disease Significant Evidence of | Respiration Disorder | Hematological Disease | Metabolic Disease | Immune System Disease | Disease Interferes with Study Subject Participation Status
Item
history, clinical or current evidence of any significant gastrointestinal, respiratory, hematological, metabolic, immunological or any other underlying disease which in the opinion of the investigator would interfere with the patient's participation in the trial;
boolean
C0017178 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0332120 (UMLS CUI [1,3])
C0035204 (UMLS CUI [2])
C0018939 (UMLS CUI [3])
C0025517 (UMLS CUI [4])
C0021053 (UMLS CUI [5])
C0012634 (UMLS CUI [6,1])
C0521102 (UMLS CUI [6,2])
C2348568 (UMLS CUI [6,3])
Hypersensitivity Angiotensin II receptor antagonist | Medical contraindication Angiotensin II receptor antagonist | Hypersensitivity Angiotensin-Converting Enzyme Inhibitors | Medical contraindication Angiotensin-Converting Enzyme Inhibitors | Hypersensitivity Allergens Cross Reactive
Item
hypersensitivity or contraindications to arbs or ace inhibitors or any cross allergy;
boolean
C0020517 (UMLS CUI [1,1])
C0521942 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0521942 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0003015 (UMLS CUI [3,2])
C1301624 (UMLS CUI [4,1])
C0003015 (UMLS CUI [4,2])
C0020517 (UMLS CUI [5,1])
C0002092 (UMLS CUI [5,2])
C0010357 (UMLS CUI [5,3])
Illicit Drugs
Item
treatment with dis-allowed medication;
boolean
C0086190 (UMLS CUI [1])
Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Inadequate
Item
pregnant or breastfeeding females or females of childbearing potential without adequate contraception;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0205412 (UMLS CUI [3,3])
Substance Use Disorders
Item
history of drug and/or alcohol abuse
boolean
C0038586 (UMLS CUI [1])
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