ID

20651

Description

GSK189075, GW869682 Or Placebo In Type 2 Diabetic Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00291356

Lien

https://clinicaltrials.gov/show/NCT00291356

Mots-clés

Versions (1)
  1. 08/03/2017 08/03/2017 -
Téléchargé le

8 mars 2017

DOI

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Licence

Creative Commons BY-NC 3.0
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Eligibility Diabetes Mellitus, Type 2 NCT00291356

Anglais

Eligibility Diabetes Mellitus, Type 2 NCT00291356

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes.
Description

Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0011860
hba1c (a measure of the average amount of sugar in blood over the last 2 or 3 months) levels are between 7.0 and 9.0.
Description

Glycosylated hemoglobin A

Type de données

boolean

Alias
UMLS CUI [1]
C0019018
taking 850mg or more per day metformin, but not taking any other diabetes medications.
Description

Metformin U/day | Antidiabetics Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0025598
UMLS CUI [1,2]
C0456683
UMLS CUI [2,1]
C0935929
UMLS CUI [2,2]
C0332197
must be medically able and willing to discontinue diabetic medications from at least 2 weeks prior to first study dose until the last study assessment.
Description

Antidiabetics Discontinue Able | Antidiabetics Discontinue Willing

Type de données

boolean

Alias
UMLS CUI [1,1]
C0935929
UMLS CUI [1,2]
C1444662
UMLS CUI [1,3]
C0085732
UMLS CUI [2,1]
C0935929
UMLS CUI [2,2]
C1444662
UMLS CUI [2,3]
C0600109
diabetic subjects who have not yet started taking diabetes medications or whose diabetes is controlled by diet alone may also be eligible to enroll if their hba1c is within 7.5 to 9.0.
Description

Antidiabetics Absent | Diabetes mellitus under control Diet | Glucohemoglobin measurement

Type de données

boolean

Alias
UMLS CUI [1,1]
C0935929
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C2062378
UMLS CUI [2,2]
C0011878
UMLS CUI [3]
C0202054
women may be eligible if they are post-menopausal or surgically sterile.
Description

Postmenopausal state | Female Sterilization

Type de données

boolean

Alias
UMLS CUI [1]
C0232970
UMLS CUI [2]
C0015787
if taking ace inhibitors, beta-blockers, calcium channel blockers, or statin type drugs, you may be eligible if your dose has been stable for at least 30 days prior to the start of the clinical trial.
Description

Angiotensin-Converting Enzyme Inhibitors Dose Stable | Adrenergic beta-1 Receptor Antagonists Dose Stable | Calcium Channel Blockers Dose Stable | Hydroxymethylglutaryl-CoA Reductase Inhibitors Dose Stable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003015
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
UMLS CUI [2,1]
C0304516
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C0205360
UMLS CUI [3,1]
C0006684
UMLS CUI [3,2]
C0178602
UMLS CUI [3,3]
C0205360
UMLS CUI [4,1]
C0360714
UMLS CUI [4,2]
C0178602
UMLS CUI [4,3]
C0205360
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
using illicit drugs, or have antibodies to hepatitis b, hepatitis c, or hiv.
Description

Illicit drug use | Hepatitis B Antibodies | Hepatitis C Antibodies | HIV Antibodies

Type de données

boolean

Alias
UMLS CUI [1]
C0281875
UMLS CUI [2]
C0019164
UMLS CUI [3]
C0166049
UMLS CUI [4]
C0019683
have any major health problems other than type 2 diabetes.
Description

Health Problem Major | Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018684
UMLS CUI [1,2]
C0033213
UMLS CUI [1,3]
C0205164
UMLS CUI [2]
C0011860
require insulin therapy or oral antidiabetic medication other than metformin.
Description

Insulin regime Patient need for | Antidiabetics Oral Patient need for | Metformin

Type de données

boolean

Alias
UMLS CUI [1,1]
C0557978
UMLS CUI [1,2]
C0686904
UMLS CUI [2,1]
C0935929
UMLS CUI [2,2]
C1527415
UMLS CUI [2,3]
C0686904
UMLS CUI [3]
C0025598
subjects who have had a urinary tract infection within 4 weeks of the start of the study or who have kidney disease.
Description

Urinary tract infection | Kidney Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0042029
UMLS CUI [2]
C0022658
subjects with either low or high blood pressure.
Description

Hypotension | Hypertensive disease

Type de données

boolean

Alias
UMLS CUI [1]
C0020649
UMLS CUI [2]
C0020538
men who are unwilling to abstain from intercourse, or use a condom with a pregnant or nursing female, or who are unwilling to use a condom with another form of contraception with a female who could become pregnant.
Description

Gender Sexual Abstinence Unwilling | Gender Male condom Unwilling | Pregnancy | Breast Feeding | Gender Contraceptive methods Unwilling

Type de données

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0036899
UMLS CUI [1,3]
C0558080
UMLS CUI [2,1]
C0079399
UMLS CUI [2,2]
C0009653
UMLS CUI [2,3]
C0558080
UMLS CUI [3]
C0032961
UMLS CUI [4]
C0006147
UMLS CUI [5,1]
C0079399
UMLS CUI [5,2]
C0700589
UMLS CUI [5,3]
C0558080
Retour au début de la page

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00291356

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent
Item
type 2 diabetes.
boolean
C0011860 (UMLS CUI [1])
Glycosylated hemoglobin A
Item
hba1c (a measure of the average amount of sugar in blood over the last 2 or 3 months) levels are between 7.0 and 9.0.
boolean
C0019018 (UMLS CUI [1])
Metformin U/day | Antidiabetics Absent
Item
taking 850mg or more per day metformin, but not taking any other diabetes medications.
boolean
C0025598 (UMLS CUI [1,1])
C0456683 (UMLS CUI [1,2])
C0935929 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Antidiabetics Discontinue Able | Antidiabetics Discontinue Willing
Item
must be medically able and willing to discontinue diabetic medications from at least 2 weeks prior to first study dose until the last study assessment.
boolean
C0935929 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C0935929 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Antidiabetics Absent | Diabetes mellitus under control Diet | Glucohemoglobin measurement
Item
diabetic subjects who have not yet started taking diabetes medications or whose diabetes is controlled by diet alone may also be eligible to enroll if their hba1c is within 7.5 to 9.0.
boolean
C0935929 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C2062378 (UMLS CUI [2,1])
C0011878 (UMLS CUI [2,2])
C0202054 (UMLS CUI [3])
Postmenopausal state | Female Sterilization
Item
women may be eligible if they are post-menopausal or surgically sterile.
boolean
C0232970 (UMLS CUI [1])
C0015787 (UMLS CUI [2])
Angiotensin-Converting Enzyme Inhibitors Dose Stable | Adrenergic beta-1 Receptor Antagonists Dose Stable | Calcium Channel Blockers Dose Stable | Hydroxymethylglutaryl-CoA Reductase Inhibitors Dose Stable
Item
if taking ace inhibitors, beta-blockers, calcium channel blockers, or statin type drugs, you may be eligible if your dose has been stable for at least 30 days prior to the start of the clinical trial.
boolean
C0003015 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0304516 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0205360 (UMLS CUI [2,3])
C0006684 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0205360 (UMLS CUI [3,3])
C0360714 (UMLS CUI [4,1])
C0178602 (UMLS CUI [4,2])
C0205360 (UMLS CUI [4,3])
Item Group
C0680251 (UMLS CUI)
Illicit drug use | Hepatitis B Antibodies | Hepatitis C Antibodies | HIV Antibodies
Item
using illicit drugs, or have antibodies to hepatitis b, hepatitis c, or hiv.
boolean
C0281875 (UMLS CUI [1])
C0019164 (UMLS CUI [2])
C0166049 (UMLS CUI [3])
C0019683 (UMLS CUI [4])
Health Problem Major | Diabetes Mellitus, Non-Insulin-Dependent
Item
have any major health problems other than type 2 diabetes.
boolean
C0018684 (UMLS CUI [1,1])
C0033213 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
C0011860 (UMLS CUI [2])
Insulin regime Patient need for | Antidiabetics Oral Patient need for | Metformin
Item
require insulin therapy or oral antidiabetic medication other than metformin.
boolean
C0557978 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
C0935929 (UMLS CUI [2,1])
C1527415 (UMLS CUI [2,2])
C0686904 (UMLS CUI [2,3])
C0025598 (UMLS CUI [3])
Urinary tract infection | Kidney Disease
Item
subjects who have had a urinary tract infection within 4 weeks of the start of the study or who have kidney disease.
boolean
C0042029 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
Hypotension | Hypertensive disease
Item
subjects with either low or high blood pressure.
boolean
C0020649 (UMLS CUI [1])
C0020538 (UMLS CUI [2])
Gender Sexual Abstinence Unwilling | Gender Male condom Unwilling | Pregnancy | Breast Feeding | Gender Contraceptive methods Unwilling
Item
men who are unwilling to abstain from intercourse, or use a condom with a pregnant or nursing female, or who are unwilling to use a condom with another form of contraception with a female who could become pregnant.
boolean
C0079399 (UMLS CUI [1,1])
C0036899 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0079399 (UMLS CUI [2,1])
C0009653 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
C0032961 (UMLS CUI [3])
C0006147 (UMLS CUI [4])
C0079399 (UMLS CUI [5,1])
C0700589 (UMLS CUI [5,2])
C0558080 (UMLS CUI [5,3])
Retour au début de la page 

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