ID

33712

Descrizione

Incretin-based Drugs and Acute Pancreatitis; ODM derived from: https://clinicaltrials.gov/show/NCT02476760

collegamento

https://clinicaltrials.gov/show/NCT02476760

Keywords

versioni (1)
  1. 20/12/18 20/12/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

20 dicembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT02476760

Inglese

Eligibility Diabetes Mellitus, Type 2 NCT02476760

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with a first-ever prescription for a non-insulin anti-diabetic drug, including biguanides, sulfonylureas, thiazolidinediones, dpp-4 inhibitors, glp-1 analogs, alpha-glucosidase inhibitors, meglitinides or combinations of these drugs from the earliest availability of data at each site to the last date of availability of data.
Descrizione

Antidiabetics Except Insulin | Biguanides | Sulfonylureas | Thiazolidinediones | DPP-4 Inhibitor | GLP-1 Analogue | alpha-Glucosidase Inhibitors | Meglitinide | Combined Modality Therapy

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0935929
UMLS CUI [1,2]
C0332300
UMLS CUI [1,3]
C0021641
UMLS CUI [2]
C0005382
UMLS CUI [3]
C0038766
UMLS CUI [4]
C1257987
UMLS CUI [5]
C3537225
UMLS CUI [6]
C3273809
UMLS CUI [7]
C1299007
UMLS CUI [8]
C0065880
UMLS CUI [9]
C0009429
patients with at least 1 year of history in the database.
Descrizione

Medical History Database Duration

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0242356
UMLS CUI [1,3]
C0449238
patients at least 18 years of age.
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who died or left the cohort before the year the first incretin-based drug entered the market.
Descrizione

Patient Outcome - Died | Cohort Withdrawal by Subject

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1546956
UMLS CUI [2,1]
C0599755
UMLS CUI [2,2]
C1710677
patients who never added-on or switched to a new anti-diabetic drug after incretin-based drugs entered the market up until june 30, 2014.
Descrizione

Absence Antidiabetics Additional | Absence Antidiabetics Change

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C0935929
UMLS CUI [1,3]
C1524062
UMLS CUI [2,1]
C0332197
UMLS CUI [2,2]
C0935929
UMLS CUI [2,3]
C0392747
patients with a previous diagnosis of pancreatic cancer, those who underwent pancreatectomy, those with diagnoses of congenital defects of the pancreas, cystic fibrosis, lupus, or previous bariatric surgery, at any time prior to study cohort entry.
Descrizione

Pancreatic carcinoma | Pancreatectomy | Congenital defects Pancreas | Cystic Fibrosis | Lupus Erythematosus | Bariatric Surgery

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0235974
UMLS CUI [2]
C0030279
UMLS CUI [3,1]
C0000768
UMLS CUI [3,2]
C0030274
UMLS CUI [4]
C0010674
UMLS CUI [5]
C0409974
UMLS CUI [6]
C1456587
patients diagnosed with hiv or initiating haart therapy before and at study cohort entry.
Descrizione

HIV Infection | HAART

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0887947
patients hospitalized for acute pancreatitis in the 30 days before study cohort entry.
Descrizione

Hospitalization Pancreatitis

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0030305
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Similar models

Eligibility Diabetes Mellitus, Type 2 NCT02476760

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Antidiabetics Except Insulin | Biguanides | Sulfonylureas | Thiazolidinediones | DPP-4 Inhibitor | GLP-1 Analogue | alpha-Glucosidase Inhibitors | Meglitinide | Combined Modality Therapy
Item
patients with a first-ever prescription for a non-insulin anti-diabetic drug, including biguanides, sulfonylureas, thiazolidinediones, dpp-4 inhibitors, glp-1 analogs, alpha-glucosidase inhibitors, meglitinides or combinations of these drugs from the earliest availability of data at each site to the last date of availability of data.
boolean
C0935929 (UMLS CUI [1,1])
C0332300 (UMLS CUI [1,2])
C0021641 (UMLS CUI [1,3])
C0005382 (UMLS CUI [2])
C0038766 (UMLS CUI [3])
C1257987 (UMLS CUI [4])
C3537225 (UMLS CUI [5])
C3273809 (UMLS CUI [6])
C1299007 (UMLS CUI [7])
C0065880 (UMLS CUI [8])
C0009429 (UMLS CUI [9])
Medical History Database Duration
Item
patients with at least 1 year of history in the database.
boolean
C0262926 (UMLS CUI [1,1])
C0242356 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Age
Item
patients at least 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Patient Outcome - Died | Cohort Withdrawal by Subject
Item
patients who died or left the cohort before the year the first incretin-based drug entered the market.
boolean
C1546956 (UMLS CUI [1])
C0599755 (UMLS CUI [2,1])
C1710677 (UMLS CUI [2,2])
Absence Antidiabetics Additional | Absence Antidiabetics Change
Item
patients who never added-on or switched to a new anti-diabetic drug after incretin-based drugs entered the market up until june 30, 2014.
boolean
C0332197 (UMLS CUI [1,1])
C0935929 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,3])
C0332197 (UMLS CUI [2,1])
C0935929 (UMLS CUI [2,2])
C0392747 (UMLS CUI [2,3])
Pancreatic carcinoma | Pancreatectomy | Congenital defects Pancreas | Cystic Fibrosis | Lupus Erythematosus | Bariatric Surgery
Item
patients with a previous diagnosis of pancreatic cancer, those who underwent pancreatectomy, those with diagnoses of congenital defects of the pancreas, cystic fibrosis, lupus, or previous bariatric surgery, at any time prior to study cohort entry.
boolean
C0235974 (UMLS CUI [1])
C0030279 (UMLS CUI [2])
C0000768 (UMLS CUI [3,1])
C0030274 (UMLS CUI [3,2])
C0010674 (UMLS CUI [4])
C0409974 (UMLS CUI [5])
C1456587 (UMLS CUI [6])
HIV Infection | HAART
Item
patients diagnosed with hiv or initiating haart therapy before and at study cohort entry.
boolean
C0019693 (UMLS CUI [1])
C0887947 (UMLS CUI [2])
Hospitalization Pancreatitis
Item
patients hospitalized for acute pancreatitis in the 30 days before study cohort entry.
boolean
C0019993 (UMLS CUI [1,1])
C0030305 (UMLS CUI [1,2])
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