ID

24084

Descripción

Comparison Between Patients With or Without Diabetes Recovery After Bariatric Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT00834938

Link

https://clinicaltrials.gov/show/NCT00834938

Palabras clave

Versiones (1)
  1. 25/7/17 25/7/17 -
Subido en

25 de julio de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Diabetes NCT00834938

Inglés

Eligibility Diabetes NCT00834938

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT00834938
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
capacity to understand the procedures of the study.
Descripción

Comprehension Study Protocol

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
to agree voluntarily to participate of the study, signing an informed consent.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
weight variance less than 5% in the last 3 months.
Descripción

Body Weight Variability

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005910
UMLS CUI [1,2]
C2827666
operative group with at least 2 year follow-up.
Descripción

Group Operative | Follow-up

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0441833
UMLS CUI [1,2]
C1882154
UMLS CUI [2]
C3274571
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of hepatic disease like cirrhosis or chronic active hepatitis.
Descripción

Liver disease | Liver Cirrhosis | Hepatitis, Chronic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0023890
UMLS CUI [3]
C0019189
kidney dysfunction (creatinine > 1,4 mg/dl in women and > 1,5 mg/dl in men).
Descripción

Abnormal renal function | Creatinine measurement, serum | Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0151746
UMLS CUI [2]
C0201976
UMLS CUI [3]
C0079399
hepatic dysfunction: alt and/or ast 3x above upper normal limit).
Descripción

Liver Dysfunction | Alanine aminotransferase increased | Aspartate aminotransferase increased

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0086565
UMLS CUI [2]
C0151905
UMLS CUI [3]
C0151904
recent history of neoplasia (< 5 years).
Descripción

Neoplastic disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1882062
use of oral or injectable for more than consecutive 14 days in the last three months.
Descripción

Oral medication | Injectables

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0175795
UMLS CUI [2]
C0086466
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Similar models

Eligibility Diabetes NCT00834938

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT00834938
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Comprehension Study Protocol
Item
capacity to understand the procedures of the study.
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
Informed Consent
Item
to agree voluntarily to participate of the study, signing an informed consent.
boolean
C0021430 (UMLS CUI [1])
Body Weight Variability
Item
weight variance less than 5% in the last 3 months.
boolean
C0005910 (UMLS CUI [1,1])
C2827666 (UMLS CUI [1,2])
Group Operative | Follow-up
Item
operative group with at least 2 year follow-up.
boolean
C0441833 (UMLS CUI [1,1])
C1882154 (UMLS CUI [1,2])
C3274571 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Liver disease | Liver Cirrhosis | Hepatitis, Chronic
Item
history of hepatic disease like cirrhosis or chronic active hepatitis.
boolean
C0023895 (UMLS CUI [1])
C0023890 (UMLS CUI [2])
C0019189 (UMLS CUI [3])
Abnormal renal function | Creatinine measurement, serum | Gender
Item
kidney dysfunction (creatinine > 1,4 mg/dl in women and > 1,5 mg/dl in men).
boolean
C0151746 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0079399 (UMLS CUI [3])
Liver Dysfunction | Alanine aminotransferase increased | Aspartate aminotransferase increased
Item
hepatic dysfunction: alt and/or ast 3x above upper normal limit).
boolean
C0086565 (UMLS CUI [1])
C0151905 (UMLS CUI [2])
C0151904 (UMLS CUI [3])
Neoplastic disease
Item
recent history of neoplasia (< 5 years).
boolean
C1882062 (UMLS CUI [1])
Oral medication | Injectables
Item
use of oral or injectable for more than consecutive 14 days in the last three months.
boolean
C0175795 (UMLS CUI [1])
C0086466 (UMLS CUI [2])
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