ID

20819

Description

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

Link

https://clinicaltrials.gov/show/NCT00221156

Keywords

Versions (1)
  1. 3/20/17 3/20/17 -
Uploaded on

March 20, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Glucose Metabolism Disorders NCT00221156

English

Eligibility Glucose Metabolism Disorders NCT00221156

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

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

Data type

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).
Description

Abnormal glucose tolerance Oral Glucose Tolerance Test

Data type

boolean

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

Glycosylated hemoglobin A Percentage

Data type

boolean

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

Age

Data type

boolean

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

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

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.
Description

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

Data type

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.
Description

Angioplasty Planned

Data type

boolean

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

Congestive heart failure Uncontrolled

Data type

boolean

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

Cerebral Infarction Episode of

Data type

boolean

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

Antidiabetics

Data type

boolean

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

Aspartate aminotransferase increased | Alanine aminotransferase increased

Data type

boolean

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

Creatinine measurement, serum

Data type

boolean

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

Ileus | Laparotomy

Data type

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.
Description

Pregnancy | Pregnancy, Planned | Breast Feeding

Data type

boolean

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

Habitual drinker Alcohol Milliliter per Day

Data type

boolean

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

Gastrectomy

Data type

boolean

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

Follow-up Time period Unsuccessful

Data type

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.
Description

Study Subject Participation Status Unsuitable for other reasons

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C3844399
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Similar models

Eligibility Glucose Metabolism Disorders NCT00221156

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
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