ID

29028

Beschrijving

Safety Study of BMS-816336 in Healthy Male Subjects; ODM derived from: https://clinicaltrials.gov/show/NCT00979368

Link

https://clinicaltrials.gov/show/NCT00979368

Trefwoorden

  1. 21-02-18 21-02-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

21 februari 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Diabetes Mellitus, Non-Insulin-Dependent NCT00979368

Eligibility Diabetes Mellitus, Non-Insulin-Dependent NCT00979368

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
healthy male subjects
Beschrijving

Healthy subject | Gender

Datatype

boolean

Alias
UMLS CUI [1]
C1708335
UMLS CUI [2]
C0079399
bmi of 18 to 32 kg/m²
Beschrijving

Body mass index

Datatype

boolean

Alias
UMLS CUI [1]
C1305855
men only, ages 18-55 years
Beschrijving

Gender | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
sexually active men not using effective birth control if their partners are wocbp
Beschrijving

Gender Sexually active | Contraceptive methods Lacking | Partner Childbearing Potential

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0241028
UMLS CUI [2,1]
C0700589
UMLS CUI [2,2]
C0332268
UMLS CUI [3,1]
C0682323
UMLS CUI [3,2]
C3831118
any significant acute or chronic medical illness
Beschrijving

Illness | Chronic disease

Datatype

boolean

Alias
UMLS CUI [1]
C0221423
UMLS CUI [2]
C0008679
family history of gilbert's disease
Beschrijving

Family history Gilbert Disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C0241889
UMLS CUI [1,2]
C0017551
history of pancreatitis
Beschrijving

Pancreatitis

Datatype

boolean

Alias
UMLS CUI [1]
C0030305
evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, egg or clinical laboratory determinations
Beschrijving

Organ dysfunction | Abnormality Physical Examination | Abnormal vital signs | Electrocardiogram abnormal | Laboratory test result abnormal

Datatype

boolean

Alias
UMLS CUI [1]
C0349410
UMLS CUI [2,1]
C1704258
UMLS CUI [2,2]
C0031809
UMLS CUI [3]
C0277804
UMLS CUI [4]
C0522055
UMLS CUI [5]
C0438215
qtc interval > 450 msec (corrected for heart rate using fridericia's correction method, qtcf)
Beschrijving

QTc interval QTcF - Fridericia's Correction Formula

Datatype

boolean

Alias
UMLS CUI [1,1]
C0489625
UMLS CUI [1,2]
C1882513
second- or third-degree a-v block or clinically relevant ecg abnormalities
Beschrijving

Second degree atrioventricular block | Complete atrioventricular block | Electrocardiogram abnormal

Datatype

boolean

Alias
UMLS CUI [1]
C0264906
UMLS CUI [2]
C0151517
UMLS CUI [3]
C0522055
history of allergy to 11-β-hsd-1 inhibitors or related compounds
Beschrijving

Hypersensitivity 11-beta-Hydroxysteroid Dehydrogenase inhibitors | Hypersensitivity Compound Related

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0044707
UMLS CUI [1,3]
C0243077
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C1706082
UMLS CUI [2,3]
C0439849
prior exposure to bms-816336
Beschrijving

Exposure to Substance Specified

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332157
UMLS CUI [1,2]
C0439861
UMLS CUI [1,3]
C0205369
use of st. john's wort (hypericum) within 4 weeks prior to the first dose of study drug and throughout the study
Beschrijving

Hypericum perforatum

Datatype

boolean

Alias
UMLS CUI [1]
C0936242
use of an oral, injectable, inhalable or suspension of glucocorticoid agents within 12 weeks of study drug administration
Beschrijving

Glucocorticoids Oral | Glucocorticoids Injectable | Glucocorticoids Inhalant | Glucocorticoids Suspension

Datatype

boolean

Alias
UMLS CUI [1,1]
C0017710
UMLS CUI [1,2]
C1527415
UMLS CUI [2,1]
C0017710
UMLS CUI [2,2]
C0086466
UMLS CUI [3,1]
C0017710
UMLS CUI [3,2]
C0001559
UMLS CUI [4,1]
C0017710
UMLS CUI [4,2]
C0038960
use of any glucocorticoid topical creams within 4 weeks of study drug administration
Beschrijving

Glucocorticoid Topical Cream

Datatype

boolean

Alias
UMLS CUI [1,1]
C0017710
UMLS CUI [1,2]
C0991551
use of oral, injectable, or topical androgen agent within 12 weeks prior to enrollment
Beschrijving

Androgen Oral | Androgen Injectable | Androgen Topical

Datatype

boolean

Alias
UMLS CUI [1,1]
C3536949
UMLS CUI [1,2]
C1527415
UMLS CUI [2,1]
C3536949
UMLS CUI [2,2]
C0086466
UMLS CUI [3,1]
C3536949
UMLS CUI [3,2]
C1522168

Similar models

Eligibility Diabetes Mellitus, Non-Insulin-Dependent NCT00979368

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Healthy subject | Gender
Item
healthy male subjects
boolean
C1708335 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Body mass index
Item
bmi of 18 to 32 kg/m²
boolean
C1305855 (UMLS CUI [1])
Gender | Age
Item
men only, ages 18-55 years
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Gender Sexually active | Contraceptive methods Lacking | Partner Childbearing Potential
Item
sexually active men not using effective birth control if their partners are wocbp
boolean
C0079399 (UMLS CUI [1,1])
C0241028 (UMLS CUI [1,2])
C0700589 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0682323 (UMLS CUI [3,1])
C3831118 (UMLS CUI [3,2])
Illness | Chronic disease
Item
any significant acute or chronic medical illness
boolean
C0221423 (UMLS CUI [1])
C0008679 (UMLS CUI [2])
Family history Gilbert Disease
Item
family history of gilbert's disease
boolean
C0241889 (UMLS CUI [1,1])
C0017551 (UMLS CUI [1,2])
Pancreatitis
Item
history of pancreatitis
boolean
C0030305 (UMLS CUI [1])
Organ dysfunction | Abnormality Physical Examination | Abnormal vital signs | Electrocardiogram abnormal | Laboratory test result abnormal
Item
evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, egg or clinical laboratory determinations
boolean
C0349410 (UMLS CUI [1])
C1704258 (UMLS CUI [2,1])
C0031809 (UMLS CUI [2,2])
C0277804 (UMLS CUI [3])
C0522055 (UMLS CUI [4])
C0438215 (UMLS CUI [5])
QTc interval QTcF - Fridericia's Correction Formula
Item
qtc interval > 450 msec (corrected for heart rate using fridericia's correction method, qtcf)
boolean
C0489625 (UMLS CUI [1,1])
C1882513 (UMLS CUI [1,2])
Second degree atrioventricular block | Complete atrioventricular block | Electrocardiogram abnormal
Item
second- or third-degree a-v block or clinically relevant ecg abnormalities
boolean
C0264906 (UMLS CUI [1])
C0151517 (UMLS CUI [2])
C0522055 (UMLS CUI [3])
Hypersensitivity 11-beta-Hydroxysteroid Dehydrogenase inhibitors | Hypersensitivity Compound Related
Item
history of allergy to 11-β-hsd-1 inhibitors or related compounds
boolean
C0020517 (UMLS CUI [1,1])
C0044707 (UMLS CUI [1,2])
C0243077 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C1706082 (UMLS CUI [2,2])
C0439849 (UMLS CUI [2,3])
Exposure to Substance Specified
Item
prior exposure to bms-816336
boolean
C0332157 (UMLS CUI [1,1])
C0439861 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Hypericum perforatum
Item
use of st. john's wort (hypericum) within 4 weeks prior to the first dose of study drug and throughout the study
boolean
C0936242 (UMLS CUI [1])
Glucocorticoids Oral | Glucocorticoids Injectable | Glucocorticoids Inhalant | Glucocorticoids Suspension
Item
use of an oral, injectable, inhalable or suspension of glucocorticoid agents within 12 weeks of study drug administration
boolean
C0017710 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0017710 (UMLS CUI [2,1])
C0086466 (UMLS CUI [2,2])
C0017710 (UMLS CUI [3,1])
C0001559 (UMLS CUI [3,2])
C0017710 (UMLS CUI [4,1])
C0038960 (UMLS CUI [4,2])
Glucocorticoid Topical Cream
Item
use of any glucocorticoid topical creams within 4 weeks of study drug administration
boolean
C0017710 (UMLS CUI [1,1])
C0991551 (UMLS CUI [1,2])
Androgen Oral | Androgen Injectable | Androgen Topical
Item
use of oral, injectable, or topical androgen agent within 12 weeks prior to enrollment
boolean
C3536949 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C3536949 (UMLS CUI [2,1])
C0086466 (UMLS CUI [2,2])
C3536949 (UMLS CUI [3,1])
C1522168 (UMLS CUI [3,2])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial