ID

33037

Beschrijving

Efficacy and Safety of Exenatide in Japanese Patients With Type 2 Diabetes Who Are Treated With Oral Antidiabetic(s); ODM derived from: https://clinicaltrials.gov/show/NCT00577824

Link

https://clinicaltrials.gov/show/NCT00577824

Trefwoorden

Versies (1)
  1. 24-11-18 24-11-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

24 november 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.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

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

Eligibility Type 2 Diabetes NCT00577824

Engels

Eligibility Type 2 Diabetes NCT00577824

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosed with type 2 diabetes.
Beschrijving

Diabetes Mellitus, Non-Insulin-Dependent

Datatype

boolean

Alias
UMLS CUI [1]
C0011860
has been treated by sulfonylurea (su) alone, su and biguanide, or su and thiazolidinedione for at least 90 days prior to study start. in a patient receiving su alone, the dose must be within the dose range from maximum maintenance dose to maximum approved dose. the patients with concomitant use of alpha glucosidase inhibitors (acarbose, voglibose or miglitol) or meglitinide derivatives (mitiglinide or nateglinide) can be included in this study, but these drugs must be discontinued at study start.
Beschrijving

Sulfonylurea | Biguanides | Thiazolidinediones | Sulfonylurea Dose Maximum Maintenance | Sulfonylurea Dose Maximum Approved | alpha-Glucosidase Inhibitors To be stopped | Acarbose To be stopped | Voglibose To be stopped | Miglitol To be stopped | Meglitinide Derivative To be stopped | Mitiglinide To be stopped | Nateglinide To be stopped

Datatype

boolean

Alias
UMLS CUI [1]
C0038766
UMLS CUI [2]
C0005382
UMLS CUI [3]
C1257987
UMLS CUI [4,1]
C0038766
UMLS CUI [4,2]
C0178602
UMLS CUI [4,3]
C0806909
UMLS CUI [4,4]
C0024501
UMLS CUI [5,1]
C0038766
UMLS CUI [5,2]
C0178602
UMLS CUI [5,3]
C0806909
UMLS CUI [5,4]
C0205540
UMLS CUI [6,1]
C1299007
UMLS CUI [6,2]
C1272691
UMLS CUI [7,1]
C0050393
UMLS CUI [7,2]
C1272691
UMLS CUI [8,1]
C0532578
UMLS CUI [8,2]
C1272691
UMLS CUI [9,1]
C0066535
UMLS CUI [9,2]
C1272691
UMLS CUI [10,1]
C0065880
UMLS CUI [10,2]
C1527240
UMLS CUI [10,3]
C1272691
UMLS CUI [11,1]
C0906166
UMLS CUI [11,2]
C1272691
UMLS CUI [12,1]
C0903898
UMLS CUI [12,2]
C1272691
have hba1c 7.0% to 10% at study start.
Beschrijving

Hemoglobin A1c measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0474680
have a body weight >=50 kg.
Beschrijving

Body Weight

Datatype

boolean

Alias
UMLS CUI [1]
C0005910
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry.
Beschrijving

Off-Label Treatment

Datatype

boolean

Alias
UMLS CUI [1]
C1096117
have participated in this study previously or any other study using exenatide or glucagon-like peptide-1 (glp-1) analogs within the last 90 days.
Beschrijving

Study Subject Participation Status | exenatide | GLP-1 analogues

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0167117
UMLS CUI [3]
C4301632
have been treated with any exogenous insulin within 90 days before study start.
Beschrijving

Insulin Exogenous

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021641
UMLS CUI [1,2]
C0205228
have been continuously treated with any drug that directly affects gastrointestinal motility for more than a total of 21 days in the 90 days prior to study start.
Beschrijving

Pharmaceutical Preparations Affecting Gastrointestinal Motility

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0017184
the combination therapy of sulfonylurea, biguanide and thiazolidinedione is not allowed.
Beschrijving

Combined Modality Therapy | Sulfonylurea | Biguanides | Thiazolidinediones

Datatype

boolean

Alias
UMLS CUI [1]
C0009429
UMLS CUI [2]
C0038766
UMLS CUI [3]
C0005382
UMLS CUI [4]
C1257987
Terug naar het begin van de pagina

Similar models

Eligibility Type 2 Diabetes NCT00577824

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent
Item
diagnosed with type 2 diabetes.
boolean
C0011860 (UMLS CUI [1])
Sulfonylurea | Biguanides | Thiazolidinediones | Sulfonylurea Dose Maximum Maintenance | Sulfonylurea Dose Maximum Approved | alpha-Glucosidase Inhibitors To be stopped | Acarbose To be stopped | Voglibose To be stopped | Miglitol To be stopped | Meglitinide Derivative To be stopped | Mitiglinide To be stopped | Nateglinide To be stopped
Item
has been treated by sulfonylurea (su) alone, su and biguanide, or su and thiazolidinedione for at least 90 days prior to study start. in a patient receiving su alone, the dose must be within the dose range from maximum maintenance dose to maximum approved dose. the patients with concomitant use of alpha glucosidase inhibitors (acarbose, voglibose or miglitol) or meglitinide derivatives (mitiglinide or nateglinide) can be included in this study, but these drugs must be discontinued at study start.
boolean
C0038766 (UMLS CUI [1])
C0005382 (UMLS CUI [2])
C1257987 (UMLS CUI [3])
C0038766 (UMLS CUI [4,1])
C0178602 (UMLS CUI [4,2])
C0806909 (UMLS CUI [4,3])
C0024501 (UMLS CUI [4,4])
C0038766 (UMLS CUI [5,1])
C0178602 (UMLS CUI [5,2])
C0806909 (UMLS CUI [5,3])
C0205540 (UMLS CUI [5,4])
C1299007 (UMLS CUI [6,1])
C1272691 (UMLS CUI [6,2])
C0050393 (UMLS CUI [7,1])
C1272691 (UMLS CUI [7,2])
C0532578 (UMLS CUI [8,1])
C1272691 (UMLS CUI [8,2])
C0066535 (UMLS CUI [9,1])
C1272691 (UMLS CUI [9,2])
C0065880 (UMLS CUI [10,1])
C1527240 (UMLS CUI [10,2])
C1272691 (UMLS CUI [10,3])
C0906166 (UMLS CUI [11,1])
C1272691 (UMLS CUI [11,2])
C0903898 (UMLS CUI [12,1])
C1272691 (UMLS CUI [12,2])
Hemoglobin A1c measurement
Item
have hba1c 7.0% to 10% at study start.
boolean
C0474680 (UMLS CUI [1])
Body Weight
Item
have a body weight >=50 kg.
boolean
C0005910 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Off-Label Treatment
Item
have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry.
boolean
C1096117 (UMLS CUI [1])
Study Subject Participation Status | exenatide | GLP-1 analogues
Item
have participated in this study previously or any other study using exenatide or glucagon-like peptide-1 (glp-1) analogs within the last 90 days.
boolean
C2348568 (UMLS CUI [1])
C0167117 (UMLS CUI [2])
C4301632 (UMLS CUI [3])
Insulin Exogenous
Item
have been treated with any exogenous insulin within 90 days before study start.
boolean
C0021641 (UMLS CUI [1,1])
C0205228 (UMLS CUI [1,2])
Pharmaceutical Preparations Affecting Gastrointestinal Motility
Item
have been continuously treated with any drug that directly affects gastrointestinal motility for more than a total of 21 days in the 90 days prior to study start.
boolean
C0013227 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0017184 (UMLS CUI [1,3])
Combined Modality Therapy | Sulfonylurea | Biguanides | Thiazolidinediones
Item
the combination therapy of sulfonylurea, biguanide and thiazolidinedione is not allowed.
boolean
C0009429 (UMLS CUI [1])
C0038766 (UMLS CUI [2])
C0005382 (UMLS CUI [3])
C1257987 (UMLS CUI [4])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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