ID

40078

Description

Effects of Low Sodium Intake on the Anti-proteinuric Efficacy in Hypertensive Patient With Olmesartan; ODM derived from: https://clinicaltrials.gov/show/NCT01552954

Lien

https://clinicaltrials.gov/show/NCT01552954

Mots-clés

Versions (1)
  1. 11/03/2020 11/03/2020 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

11 mars 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Hypertension NCT01552954

Anglais

Eligibility Hypertension NCT01552954

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 19 years or more and 75 years or less
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
hypertension patients: patients whose blood pressure is 140/90mmhg and over, patients is newly diagnosed with hypertension or is prescribed antihypertensive medications.
Description

Hypertensive disease | Blood pressure determination | Hypertensive disease Newly Diagnosed | Antihypertensive Agents prescribed

Type de données

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C0005824
UMLS CUI [3,1]
C0020538
UMLS CUI [3,2]
C1518321
UMLS CUI [4,1]
C0003364
UMLS CUI [4,2]
C0278329
hypertensive patients verified 2 times or more of albuminuria 30 mg/g cr or more in a spot urine sample with interval of 1 week or more in recent 6 months
Description

Hypertensive disease | Albuminuria Spot urine sample

Type de données

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2,1]
C0001925
UMLS CUI [2,2]
C0457208
estimated glomerular filtration rate (gfr) by modification of diet in renal disease (mdrd) equation 30 ml/min/1.73 m2 or more
Description

GFR estimation by MDRD

Type de données

boolean

Alias
UMLS CUI [1]
C2170215
patients who give written consent to this study by oneself
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
blood pressure more than 160/100 mmhg
Description

Blood pressure determination

Type de données

boolean

Alias
UMLS CUI [1]
C0005824
pregnant
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
serum potassium level more than 5.5 meq/l at screening period
Description

Serum potassium measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0302353
patients with malignancy, acute cerebral infarction, acute myocardial infarction, unstable angina, percutaneous coronary arterial intervention (pci), or coronary artery bypass graft (cabg) in recent 6 months
Description

Malignant Neoplasms | Cerebral Infarction | Myocardial Infarction | Angina, Unstable | Percutaneous Coronary Intervention | Coronary Artery Bypass Surgery

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0007785
UMLS CUI [3]
C0027051
UMLS CUI [4]
C0002965
UMLS CUI [5]
C1532338
UMLS CUI [6]
C0010055
patients with diabetes mellitus
Description

Diabetes Mellitus

Type de données

boolean

Alias
UMLS CUI [1]
C0011849
patients who have an allergy to olmesartan
Description

Hypersensitivity Olmesartan

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1098320
patients who were involved in other clinical trial in recent 1 month or are participated in screening period
Description

Study Subject Participation Status | Clinical Trial | Trial Screening

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0008976
UMLS CUI [3]
C1710477
patients taking medication(s) of corticosteroid or immunosuppressant in a screening period
Description

Adrenal Cortex Hormones | Immunosuppressive Agents

Type de données

boolean

Alias
UMLS CUI [1]
C0001617
UMLS CUI [2]
C0021081
Retour au début de la page

Similar models

Eligibility Hypertension NCT01552954

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
aged 19 years or more and 75 years or less
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease | Blood pressure determination | Hypertensive disease Newly Diagnosed | Antihypertensive Agents prescribed
Item
hypertension patients: patients whose blood pressure is 140/90mmhg and over, patients is newly diagnosed with hypertension or is prescribed antihypertensive medications.
boolean
C0020538 (UMLS CUI [1])
C0005824 (UMLS CUI [2])
C0020538 (UMLS CUI [3,1])
C1518321 (UMLS CUI [3,2])
C0003364 (UMLS CUI [4,1])
C0278329 (UMLS CUI [4,2])
Hypertensive disease | Albuminuria Spot urine sample
Item
hypertensive patients verified 2 times or more of albuminuria 30 mg/g cr or more in a spot urine sample with interval of 1 week or more in recent 6 months
boolean
C0020538 (UMLS CUI [1])
C0001925 (UMLS CUI [2,1])
C0457208 (UMLS CUI [2,2])
GFR estimation by MDRD
Item
estimated glomerular filtration rate (gfr) by modification of diet in renal disease (mdrd) equation 30 ml/min/1.73 m2 or more
boolean
C2170215 (UMLS CUI [1])
Informed Consent
Item
patients who give written consent to this study by oneself
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Blood pressure determination
Item
blood pressure more than 160/100 mmhg
boolean
C0005824 (UMLS CUI [1])
Pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])
Serum potassium measurement
Item
serum potassium level more than 5.5 meq/l at screening period
boolean
C0302353 (UMLS CUI [1])
Malignant Neoplasms | Cerebral Infarction | Myocardial Infarction | Angina, Unstable | Percutaneous Coronary Intervention | Coronary Artery Bypass Surgery
Item
patients with malignancy, acute cerebral infarction, acute myocardial infarction, unstable angina, percutaneous coronary arterial intervention (pci), or coronary artery bypass graft (cabg) in recent 6 months
boolean
C0006826 (UMLS CUI [1])
C0007785 (UMLS CUI [2])
C0027051 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C1532338 (UMLS CUI [5])
C0010055 (UMLS CUI [6])
Diabetes Mellitus
Item
patients with diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Hypersensitivity Olmesartan
Item
patients who have an allergy to olmesartan
boolean
C0020517 (UMLS CUI [1,1])
C1098320 (UMLS CUI [1,2])
Study Subject Participation Status | Clinical Trial | Trial Screening
Item
patients who were involved in other clinical trial in recent 1 month or are participated in screening period
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
C1710477 (UMLS CUI [3])
Adrenal Cortex Hormones | Immunosuppressive Agents
Item
patients taking medication(s) of corticosteroid or immunosuppressant in a screening period
boolean
C0001617 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
Retour au début de la page 

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