ID

17688

Description

Glucose Optimisation With Angiotensin II Antagonist Losartan (GOAAL); ODM derived from: https://clinicaltrials.gov/show/NCT00237588

Lien

https://clinicaltrials.gov/show/NCT00237588

Mots-clés

Versions (1)
  1. 28/09/2016 28/09/2016 -
Téléchargé le

28 septembre 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Hypertension NCT00237588

Anglais

Eligibility Hypertension NCT00237588

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
essential hypertension with diastolic blood pressure 95-110 mmhg and systolic blood pressure < 180 mmhg
Description

Essential Hypertension | Diastolic blood pressure | Systolic Pressure

Type de données

boolean

Alias
UMLS CUI [1]
C0085580
UMLS CUI [2]
C0428883
UMLS CUI [3]
C0871470
previously untreated hypertension or treated with monotherapy (but not with ace-inhibitors or angiotensin ii-receptor blockers)
Description

hypertension untreated | Therapeutic procedure Hypertensive disease | Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist

Type de données

boolean

Alias
UMLS CUI [1]
C0745134
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0020538
UMLS CUI [3]
C0003015
UMLS CUI [4]
C0521942
impaired glucose tolerance or impaired fasting glucose (fasting plasma glucose; 6.1-7.0 mmol/l (110-126 mg/dl)
Description

Impaired glucose tolerance | Impaired fasting glycaemia | Plasma fasting glucose measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0271650
UMLS CUI [2]
C1272092
UMLS CUI [3]
C0583513
age over 18
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
any one of these: microalbuminuria (urin excretion >20 microg/min), dyslipidemia (hdl-cholesterol <0.9 mmol/l(35 mg/dl), triglycerides > 1.7 mmol/l (150 mg/dl), waist to hip-ratio >0.9 in men and >0.85 in women, bmi >28 kg/m2.
Description

Microalbuminuria | Dyslipidemias | Serum HDL cholesterol measurement | Triglycerides measurement | Waist-Hip Ratio | Gender | Body mass index

Type de données

boolean

Alias
UMLS CUI [1]
C0730345
UMLS CUI [2]
C0242339
UMLS CUI [3]
C0428472
UMLS CUI [4]
C0202236
UMLS CUI [5]
C0205682
UMLS CUI [6]
C0079399
UMLS CUI [7]
C1305855
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous or current use of ace-inhibitors or angiotensin ii-receptor blockers
Description

Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist

Type de données

boolean

Alias
UMLS CUI [1]
C0003015
UMLS CUI [2]
C0521942
previous or current antidiabetic medications
Description

Antidiabetics

Type de données

boolean

Alias
UMLS CUI [1]
C0935929
"brittle" pre-diabetes where the investigator anticipates pharmacological treatment within next 6 months
Description

Prediabetes syndrome | Pharmacotherapy Anticipated

Type de données

boolean

Alias
UMLS CUI [1]
C0362046
UMLS CUI [2,1]
C0013216
UMLS CUI [2,2]
C3840775
hypertensive patients where the investigator anticipates polytherapy within next 6 months
Description

Hypertensive | Combination Drug Therapy Anticipated

Type de données

boolean

Alias
UMLS CUI [1]
C0857121
UMLS CUI [2,1]
C0013218
UMLS CUI [2,2]
C3840775
female patient who is pregnant or nursing or planning pregnancy within the duration of the study
Description

Pregnancy | Breast Feeding | Pregnancy, Planned

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
Retour au début de la page

Similar models

Eligibility Hypertension NCT00237588

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Essential Hypertension | Diastolic blood pressure | Systolic Pressure
Item
essential hypertension with diastolic blood pressure 95-110 mmhg and systolic blood pressure < 180 mmhg
boolean
C0085580 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0871470 (UMLS CUI [3])
hypertension untreated | Therapeutic procedure Hypertensive disease | Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist
Item
previously untreated hypertension or treated with monotherapy (but not with ace-inhibitors or angiotensin ii-receptor blockers)
boolean
C0745134 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0020538 (UMLS CUI [2,2])
C0003015 (UMLS CUI [3])
C0521942 (UMLS CUI [4])
Impaired glucose tolerance | Impaired fasting glycaemia | Plasma fasting glucose measurement
Item
impaired glucose tolerance or impaired fasting glucose (fasting plasma glucose; 6.1-7.0 mmol/l (110-126 mg/dl)
boolean
C0271650 (UMLS CUI [1])
C1272092 (UMLS CUI [2])
C0583513 (UMLS CUI [3])
Age
Item
age over 18
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Microalbuminuria | Dyslipidemias | Serum HDL cholesterol measurement | Triglycerides measurement | Waist-Hip Ratio | Gender | Body mass index
Item
any one of these: microalbuminuria (urin excretion >20 microg/min), dyslipidemia (hdl-cholesterol <0.9 mmol/l(35 mg/dl), triglycerides > 1.7 mmol/l (150 mg/dl), waist to hip-ratio >0.9 in men and >0.85 in women, bmi >28 kg/m2.
boolean
C0730345 (UMLS CUI [1])
C0242339 (UMLS CUI [2])
C0428472 (UMLS CUI [3])
C0202236 (UMLS CUI [4])
C0205682 (UMLS CUI [5])
C0079399 (UMLS CUI [6])
C1305855 (UMLS CUI [7])
Item Group
C0680251 (UMLS CUI)
Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist
Item
previous or current use of ace-inhibitors or angiotensin ii-receptor blockers
boolean
C0003015 (UMLS CUI [1])
C0521942 (UMLS CUI [2])
Antidiabetics
Item
previous or current antidiabetic medications
boolean
C0935929 (UMLS CUI [1])
Prediabetes syndrome | Pharmacotherapy Anticipated
Item
"brittle" pre-diabetes where the investigator anticipates pharmacological treatment within next 6 months
boolean
C0362046 (UMLS CUI [1])
C0013216 (UMLS CUI [2,1])
C3840775 (UMLS CUI [2,2])
Hypertensive | Combination Drug Therapy Anticipated
Item
hypertensive patients where the investigator anticipates polytherapy within next 6 months
boolean
C0857121 (UMLS CUI [1])
C0013218 (UMLS CUI [2,1])
C3840775 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
female patient who is pregnant or nursing or planning pregnancy within the duration of the study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Retour au début de la page 

Contact

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Aide

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial