ID

40119

Description

Value of Liquid Potassium Magnesium Citrate in Controlling Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01682837

Lien

https://clinicaltrials.gov/show/NCT01682837

Mots-clés

  1. 12/03/2020 12/03/2020 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

12 mars 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Hypertension NCT01682837

Eligibility Hypertension NCT01682837

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
men or women > 21 years of age
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
any race/ethnicity
Description

Racial group Any | Ethnicity Any

Type de données

boolean

Alias
UMLS CUI [1,1]
C0034510
UMLS CUI [1,2]
C1552551
UMLS CUI [2,1]
C0015031
UMLS CUI [2,2]
C1552551
pre- or stage i hypertension (bp >= 120/80 and <= 159/99)
Description

Prehypertension | Hypertensive disease Stage | Blood pressure determination

Type de données

boolean

Alias
UMLS CUI [1]
C1696708
UMLS CUI [2,1]
C0020538
UMLS CUI [2,2]
C0699749
UMLS CUI [3]
C0005824
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
diabetes mellitus
Description

Diabetes Mellitus

Type de données

boolean

Alias
UMLS CUI [1]
C0011849
renal impairment (serum creatinine > 1.4 mg/dl)
Description

Renal Insufficiency | Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1]
C1565489
UMLS CUI [2]
C0201976
any heart diseases such as congestive heart failure or sustained arrhythmia
Description

Heart Diseases | Congestive heart failure | Cardiac Arrhythmia Sustained

Type de données

boolean

Alias
UMLS CUI [1]
C0018799
UMLS CUI [2]
C0018802
UMLS CUI [3,1]
C0003811
UMLS CUI [3,2]
C0443318
chronic nsaid use
Description

NSAID chronic

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003211
UMLS CUI [1,2]
C0205191
treatment with diuretics
Description

Diuretic therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0948575
gastroesophageal reflux disease (gerd) requiring treatment with acid reducing agents or antacid more than once a week
Description

Gastroesophageal reflux disease Requirement Antacids | Antacids times/week

Type de données

boolean

Alias
UMLS CUI [1,1]
C0017168
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0003138
UMLS CUI [2,1]
C0003138
UMLS CUI [2,2]
C0456698
esophageal-gastric ulcer
Description

Ulcer of esophagus | Gastric ulcer

Type de données

boolean

Alias
UMLS CUI [1]
C0151970
UMLS CUI [2]
C0038358
chronic diarrhea
Description

Chronic diarrhea

Type de données

boolean

Alias
UMLS CUI [1]
C0401151
hyperkalemia (serum > 4.6 meq/l for patients on ace inhibitors or arbs, serum k > 5.0 for patient not on ace inhibitors or arbs)
Description

Hyperkalemia | Serum potassium measurement | Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist | Angiotensin-Converting Enzyme Inhibitors Absent | Angiotensin II receptor antagonist Absent

Type de données

boolean

Alias
UMLS CUI [1]
C0020461
UMLS CUI [2]
C0302353
UMLS CUI [3]
C0003015
UMLS CUI [4]
C0521942
UMLS CUI [5,1]
C0003015
UMLS CUI [5,2]
C0332197
UMLS CUI [6,1]
C0521942
UMLS CUI [6,2]
C0332197
abnormal liver function test (ast or alt above upper limit of normal range)
Description

Liver function tests abnormal | Aspartate aminotransferase increased | Alanine aminotransferase increased

Type de données

boolean

Alias
UMLS CUI [1]
C0151766
UMLS CUI [2]
C0151904
UMLS CUI [3]
C0151905
subjects who require any potassium supplement on a regular basis from any reasons
Description

Requirement Potassium supplement Regular

Type de données

boolean

Alias
UMLS CUI [1,1]
C1514873
UMLS CUI [1,2]
C0304475
UMLS CUI [1,3]
C0205272
pregnancy
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
history of major depression, bipolar disorder, or schizophrenia
Description

Major Depressive Disorder | Bipolar Disorder | Schizophrenia

Type de données

boolean

Alias
UMLS CUI [1]
C1269683
UMLS CUI [2]
C0005586
UMLS CUI [3]
C0036341

Similar models

Eligibility Hypertension NCT01682837

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
men or women > 21 years of age
boolean
C0001779 (UMLS CUI [1])
Racial group Any | Ethnicity Any
Item
any race/ethnicity
boolean
C0034510 (UMLS CUI [1,1])
C1552551 (UMLS CUI [1,2])
C0015031 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
Prehypertension | Hypertensive disease Stage | Blood pressure determination
Item
pre- or stage i hypertension (bp >= 120/80 and <= 159/99)
boolean
C1696708 (UMLS CUI [1])
C0020538 (UMLS CUI [2,1])
C0699749 (UMLS CUI [2,2])
C0005824 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus
Item
diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Renal Insufficiency | Creatinine measurement, serum
Item
renal impairment (serum creatinine > 1.4 mg/dl)
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Heart Diseases | Congestive heart failure | Cardiac Arrhythmia Sustained
Item
any heart diseases such as congestive heart failure or sustained arrhythmia
boolean
C0018799 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
C0003811 (UMLS CUI [3,1])
C0443318 (UMLS CUI [3,2])
NSAID chronic
Item
chronic nsaid use
boolean
C0003211 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
Diuretic therapy
Item
treatment with diuretics
boolean
C0948575 (UMLS CUI [1])
Gastroesophageal reflux disease Requirement Antacids | Antacids times/week
Item
gastroesophageal reflux disease (gerd) requiring treatment with acid reducing agents or antacid more than once a week
boolean
C0017168 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0003138 (UMLS CUI [1,3])
C0003138 (UMLS CUI [2,1])
C0456698 (UMLS CUI [2,2])
Ulcer of esophagus | Gastric ulcer
Item
esophageal-gastric ulcer
boolean
C0151970 (UMLS CUI [1])
C0038358 (UMLS CUI [2])
Chronic diarrhea
Item
chronic diarrhea
boolean
C0401151 (UMLS CUI [1])
Hyperkalemia | Serum potassium measurement | Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist | Angiotensin-Converting Enzyme Inhibitors Absent | Angiotensin II receptor antagonist Absent
Item
hyperkalemia (serum > 4.6 meq/l for patients on ace inhibitors or arbs, serum k > 5.0 for patient not on ace inhibitors or arbs)
boolean
C0020461 (UMLS CUI [1])
C0302353 (UMLS CUI [2])
C0003015 (UMLS CUI [3])
C0521942 (UMLS CUI [4])
C0003015 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
C0521942 (UMLS CUI [6,1])
C0332197 (UMLS CUI [6,2])
Liver function tests abnormal | Aspartate aminotransferase increased | Alanine aminotransferase increased
Item
abnormal liver function test (ast or alt above upper limit of normal range)
boolean
C0151766 (UMLS CUI [1])
C0151904 (UMLS CUI [2])
C0151905 (UMLS CUI [3])
Requirement Potassium supplement Regular
Item
subjects who require any potassium supplement on a regular basis from any reasons
boolean
C1514873 (UMLS CUI [1,1])
C0304475 (UMLS CUI [1,2])
C0205272 (UMLS CUI [1,3])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Major Depressive Disorder | Bipolar Disorder | Schizophrenia
Item
history of major depression, bipolar disorder, or schizophrenia
boolean
C1269683 (UMLS CUI [1])
C0005586 (UMLS CUI [2])
C0036341 (UMLS CUI [3])

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