ID

17688

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT00237588

Stichworte

  1. 28.09.16 28.09.16 -
Hochgeladen am

28. September 2016

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Hypertension NCT00237588

Eligibility Hypertension NCT00237588

Inclusion Criteria
Beschreibung

Inclusion Criteria

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

Essential Hypertension | Diastolic blood pressure | Systolic Pressure

Datentyp

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)
Beschreibung

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

Datentyp

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)
Beschreibung

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

Datentyp

boolean

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

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
informed consent
Beschreibung

Informed Consent

Datentyp

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.
Beschreibung

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

Datentyp

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
Beschreibung

Exclusion Criteria

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

Angiotensin-Converting Enzyme Inhibitors | Angiotensin II receptor antagonist

Datentyp

boolean

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

Antidiabetics

Datentyp

boolean

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

Prediabetes syndrome | Pharmacotherapy Anticipated

Datentyp

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
Beschreibung

Hypertensive | Combination Drug Therapy Anticipated

Datentyp

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
Beschreibung

Pregnancy | Breast Feeding | Pregnancy, Planned

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992

Ähnliche Modelle

Eligibility Hypertension NCT00237588

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video