ID

20819

Beschreibung

Acarbose and Secondary Prevention After Coronary Stenting; ODM derived from: https://clinicaltrials.gov/show/NCT00221156

Link

https://clinicaltrials.gov/show/NCT00221156

Stichworte

Versionen (1)
  1. 20.03.17 20.03.17 -
Hochgeladen am

20. März 2017

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.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

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

Eligibility Glucose Metabolism Disorders NCT00221156

Englisch

Eligibility Glucose Metabolism Disorders NCT00221156

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
within 8 weeks since implantation of coronary artery stents for stable angina pectoris or acute coronary syndrome.
Beschreibung

Placement of stent in coronary artery | Stable angina | Acute Coronary Syndrome

Datentyp

boolean

Alias
UMLS CUI [1]
C0521232
UMLS CUI [2]
C0340288
UMLS CUI [3]
C0948089
abnormal glucose tolerance according to a 75 g oral glucose tolerance test (ogtt).
Beschreibung

Abnormal glucose tolerance Oral Glucose Tolerance Test

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0235401
UMLS CUI [1,2]
C0029161
hba1c is less than 6.5%.
Beschreibung

Glycosylated hemoglobin A Percentage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0019018
UMLS CUI [1,2]
C0439165
age is between 20 and 75 years (at time of consent).
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
patients who can give informed consent themselves in writing.
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with abnormal glucose tolerance caused by other organic disorders such as pancreatitis, hemochromatosis, post pancreatectomy, hyperthyroidism, cushing syndrome, prader-willi syndrome, etc.
Beschreibung

Abnormal glucose tolerance caused by organic disease | Pancreatitis | Hemochromatosis | Pancreatectomy Status post | Hyperthyroidism | Cushing Syndrome | Prader-Willi Syndrome

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0235401
UMLS CUI [1,2]
C0015127
UMLS CUI [1,3]
C0683324
UMLS CUI [2]
C0030305
UMLS CUI [3]
C0018995
UMLS CUI [4,1]
C0030279
UMLS CUI [4,2]
C0687676
UMLS CUI [5]
C0020550
UMLS CUI [6]
C0010481
UMLS CUI [7]
C0032897
patients with planned angioplasty.
Beschreibung

Angioplasty Planned

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0162577
UMLS CUI [1,2]
C1301732
patients with uncontrollable congestive heart failure.
Beschreibung

Congestive heart failure Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0205318
less than 6 months since last episode of cerebral infarction.
Beschreibung

Cerebral Infarction Episode of

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007785
UMLS CUI [1,2]
C0332189
patients who have received medication for diabetes mellitus before.
Beschreibung

Antidiabetics

Datentyp

boolean

Alias
UMLS CUI [1]
C0935929
ast (got) exceeding 100 iu/l or alt (gpt) exceeding 100 iu/l.
Beschreibung

Aspartate aminotransferase increased | Alanine aminotransferase increased

Datentyp

boolean

Alias
UMLS CUI [1]
C0151904
UMLS CUI [2]
C0151905
creatinine exceeding 2 mg/dl.
Beschreibung

Creatinine measurement, serum

Datentyp

boolean

Alias
UMLS CUI [1]
C0201976
patients with a history of ileus or less than 6 months since celiotomy.
Beschreibung

Ileus | Laparotomy

Datentyp

boolean

Alias
UMLS CUI [1]
C1258215
UMLS CUI [2]
C0023038
pregnant women or those who plan to become pregnant, or are in the lactation period.
Beschreibung

Pregnancy | Pregnancy, Planned | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
UMLS CUI [3]
C0006147
habitual drinker (more than 100 ml/day of alcohol).
Beschreibung

Habitual drinker Alcohol Milliliter per Day

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0556340
UMLS CUI [1,2]
C0001948
UMLS CUI [1,3]
C0439446
patients with a history of gastrectomy.
Beschreibung

Gastrectomy

Datentyp

boolean

Alias
UMLS CUI [1]
C0017118
patients for whom it is impossible to follow up for 5 years.
Beschreibung

Follow-up Time period Unsuccessful

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1948053
UMLS CUI [1,3]
C1272705
any other reason that the clinical supervisors or clinical researchers may have for considering a case unsuitable for the study.
Beschreibung

Study Subject Participation Status Unsuitable for other reasons

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C3844399
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Glucose Metabolism Disorders NCT00221156

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Placement of stent in coronary artery | Stable angina | Acute Coronary Syndrome
Item
within 8 weeks since implantation of coronary artery stents for stable angina pectoris or acute coronary syndrome.
boolean
C0521232 (UMLS CUI [1])
C0340288 (UMLS CUI [2])
C0948089 (UMLS CUI [3])
Abnormal glucose tolerance Oral Glucose Tolerance Test
Item
abnormal glucose tolerance according to a 75 g oral glucose tolerance test (ogtt).
boolean
C0235401 (UMLS CUI [1,1])
C0029161 (UMLS CUI [1,2])
Glycosylated hemoglobin A Percentage
Item
hba1c is less than 6.5%.
boolean
C0019018 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
Age
Item
age is between 20 and 75 years (at time of consent).
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
patients who can give informed consent themselves in writing.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Abnormal glucose tolerance caused by organic disease | Pancreatitis | Hemochromatosis | Pancreatectomy Status post | Hyperthyroidism | Cushing Syndrome | Prader-Willi Syndrome
Item
patients with abnormal glucose tolerance caused by other organic disorders such as pancreatitis, hemochromatosis, post pancreatectomy, hyperthyroidism, cushing syndrome, prader-willi syndrome, etc.
boolean
C0235401 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0683324 (UMLS CUI [1,3])
C0030305 (UMLS CUI [2])
C0018995 (UMLS CUI [3])
C0030279 (UMLS CUI [4,1])
C0687676 (UMLS CUI [4,2])
C0020550 (UMLS CUI [5])
C0010481 (UMLS CUI [6])
C0032897 (UMLS CUI [7])
Angioplasty Planned
Item
patients with planned angioplasty.
boolean
C0162577 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Congestive heart failure Uncontrolled
Item
patients with uncontrollable congestive heart failure.
boolean
C0018802 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Cerebral Infarction Episode of
Item
less than 6 months since last episode of cerebral infarction.
boolean
C0007785 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
Antidiabetics
Item
patients who have received medication for diabetes mellitus before.
boolean
C0935929 (UMLS CUI [1])
Aspartate aminotransferase increased | Alanine aminotransferase increased
Item
ast (got) exceeding 100 iu/l or alt (gpt) exceeding 100 iu/l.
boolean
C0151904 (UMLS CUI [1])
C0151905 (UMLS CUI [2])
Creatinine measurement, serum
Item
creatinine exceeding 2 mg/dl.
boolean
C0201976 (UMLS CUI [1])
Ileus | Laparotomy
Item
patients with a history of ileus or less than 6 months since celiotomy.
boolean
C1258215 (UMLS CUI [1])
C0023038 (UMLS CUI [2])
Pregnancy | Pregnancy, Planned | Breast Feeding
Item
pregnant women or those who plan to become pregnant, or are in the lactation period.
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Habitual drinker Alcohol Milliliter per Day
Item
habitual drinker (more than 100 ml/day of alcohol).
boolean
C0556340 (UMLS CUI [1,1])
C0001948 (UMLS CUI [1,2])
C0439446 (UMLS CUI [1,3])
Gastrectomy
Item
patients with a history of gastrectomy.
boolean
C0017118 (UMLS CUI [1])
Follow-up Time period Unsuccessful
Item
patients for whom it is impossible to follow up for 5 years.
boolean
C3274571 (UMLS CUI [1,1])
C1948053 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Study Subject Participation Status Unsuitable for other reasons
Item
any other reason that the clinical supervisors or clinical researchers may have for considering a case unsuitable for the study.
boolean
C2348568 (UMLS CUI [1,1])
C3844399 (UMLS CUI [1,2])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

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