Age Legal
Item
patients with legal age
boolean
C0001779 (UMLS CUI [1,1])
C1301860 (UMLS CUI [1,2])
Body mass index
Item
body mass index >27kg/m2
boolean
C1305855 (UMLS CUI [1])
Non-Insulin-Dependent Diabetes Mellitus WHO classification | Metformin | Metformin Dose Stable U/day
Item
type 2 diabetes as defined by who criteria, treated with metformin for at least 6 months and with a stable dose of metformin >=1500 mg/day for at least three months
boolean
C0011860 (UMLS CUI [1,1])
C4267671 (UMLS CUI [1,2])
C0025598 (UMLS CUI [2])
C0025598 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0205360 (UMLS CUI [3,3])
C0456683 (UMLS CUI [3,4])
Glucohemoglobin measurement
Item
hba1c >=7% and <=9% at screening visit
boolean
C0202054 (UMLS CUI [1])
Weight decreased Quantity Duration
Item
weight loss > 5 kg within three months prior to screening
boolean
C1262477 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Endocrine System Diseases
Item
presence of any clinically significant endocrine disease according to the investigator
boolean
C0014130 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent
Item
presence of type 1 diabetes
boolean
C0011854 (UMLS CUI [1])
Malignant Neoplasms | Exception Basal cell carcinoma Localized Treated | Exception Carcinoma in situ of uterine cervix Treated
Item
presence or history of cancer within the past 5 years with the exception of adequately-treated localized basal cell skin cancer or in situ uterine cervical cancer
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])
C0392752 (UMLS CUI [2,3])
C1522326 (UMLS CUI [2,4])
C1705847 (UMLS CUI [3,1])
C0851140 (UMLS CUI [3,2])
C1522326 (UMLS CUI [3,3])
Study Subject Participation Status | rimonabant
Item
previous participation in a clinical study with rimonabant
boolean
C2348568 (UMLS CUI [1])
C1142933 (UMLS CUI [2])
Childbearing Potential Contraceptive methods Absent
Item
absence of effective medical contraceptive method for females of childbearing potential
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Antidiabetics Oral | Exception Metformin | Insulin | Anti-Obesity Agents | Weight-Loss Agents
Item
within 3 months prior to screening visit: use of oral antidiabetic drugs (other than metformin) and/or insulin, of anti-obesity drugs or other drugs for weight reduction
boolean
C0935929 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0025598 (UMLS CUI [2,2])
C0021641 (UMLS CUI [3])
C0376607 (UMLS CUI [4])
C0376606 (UMLS CUI [5])
CORTICOSTEROIDS FOR SYSTEMIC USE Active Long-term | CORTICOSTEROIDS SYSTEMIC Use Prolonged | Lipid-lowering therapy Change
Item
within 2 months prior to screening visit: administration of systemic long-acting corticosteroids or prolonged use (more than one week) of other systemic corticosteroids, change in lipid lowering treatment
boolean
C3653708 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])
C0443252 (UMLS CUI [1,3])
C3653708 (UMLS CUI [2,1])
C1524063 (UMLS CUI [2,2])
C0439590 (UMLS CUI [2,3])
C0585943 (UMLS CUI [3,1])
C0392747 (UMLS CUI [3,2])
Medical condition Severe compromises Patient safety | Medical condition Severe compromises Study Subject Participation Status | Severe Mental Disorders compromise Patient safety | Severe Mental Disorders compromise Study Subject Participation Status | Chronic disease compromises Patient safety | Chronic disease compromises Study Subject Participation Status | Chronic infectious disease compromises Patient safety | Chronic infectious disease compromises Study Subject Participation Status
Item
presence of any severe medical or psychological condition or chronic conditions/infections that in the opinion of the investigator would compromise the patient's safety or successful participation in the study, including uncontrolled serious psychiatric illness
boolean
C3843040 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2945640 (UMLS CUI [1,3])
C1113679 (UMLS CUI [1,4])
C3843040 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C2945640 (UMLS CUI [2,3])
C2348568 (UMLS CUI [2,4])
C4046029 (UMLS CUI [3,1])
C2945640 (UMLS CUI [3,2])
C1113679 (UMLS CUI [3,3])
C4046029 (UMLS CUI [4,1])
C2945640 (UMLS CUI [4,2])
C2348568 (UMLS CUI [4,3])
C0008679 (UMLS CUI [5,1])
C2945640 (UMLS CUI [5,2])
C1113679 (UMLS CUI [5,3])
C0008679 (UMLS CUI [6,1])
C2945640 (UMLS CUI [6,2])
C2348568 (UMLS CUI [6,3])
C0151317 (UMLS CUI [7,1])
C2945640 (UMLS CUI [7,2])
C1113679 (UMLS CUI [7,3])
C0151317 (UMLS CUI [8,1])
C2945640 (UMLS CUI [8,2])
C2348568 (UMLS CUI [8,3])
Study Subject Participation Status Aspect Additional
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean
C2348568 (UMLS CUI [1,1])
C1879746 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,3])