ID

13094

Description

Beta-Cell Transplantation in Pre-Uremic Patients With Type 1 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00623610

Lien

https://clinicaltrials.gov/show/NCT00623610

Mots-clés

  1. 15/01/2016 15/01/2016 -
Téléchargé le

15 janvier 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 1 NCT00623610

Eligibility Diabetes Mellitus, Type 1 NCT00623610

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 1 insulin-dependent diabetic patients in relatively good general condition
Description

type 1 diabetes, health status

Type de données

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0018759
non-smoker
Description

tobacco use

Type de données

boolean

Alias
UMLS CUI [1]
C0543414
body weight < 80 kg
Description

weight

Type de données

boolean

Alias
UMLS CUI [1]
C0005910
c-peptide < 0.03 nmol/l (<0.09 µg/l) 6 min. after glucagon iv (1mg) (glycemia > 180 mg/dl)
Description

c-peptide after glucagon

Type de données

boolean

Alias
UMLS CUI [1,1]
C0202100
UMLS CUI [1,2]
C0332282
UMLS CUI [1,3]
C0017687
ebv antibody positive
Description

ebv antibody positive

Type de données

boolean

Alias
UMLS CUI [1]
C0241883
cooperative and reliable patient giving informed consent by signature; the patient should be informed in sufficient detail on the content and procedure of the protocol, indicating potential risks of intervention and of immunosuppressive therapy; the patient should also be informed that withdrawal of immunosuppressive therapy in patients with persistent plasma c-peptide positivity may result in subsequent loss of ß-cell graft function; the ß cell implant should be identified as a clinical trial.
Description

informed consent, compliance

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C1321605
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of thrombosis or pulmonary embolism
Description

thrombosis, pulmonary embolism

Type de données

boolean

Alias
UMLS CUI [1]
C0040053
UMLS CUI [2]
C0034065
abnormal liver function
Description

liver dysfunction

Type de données

boolean

Alias
UMLS CUI [1]
C0086565
hla antibodies
Description

hla antibodies

Type de données

boolean

Alias
UMLS CUI [1]
C0024284

Similar models

Eligibility Diabetes Mellitus, Type 1 NCT00623610

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
type 1 diabetes, health status
Item
type 1 insulin-dependent diabetic patients in relatively good general condition
boolean
C0011854 (UMLS CUI [1])
C0018759 (UMLS CUI [2])
tobacco use
Item
non-smoker
boolean
C0543414 (UMLS CUI [1])
weight
Item
body weight < 80 kg
boolean
C0005910 (UMLS CUI [1])
c-peptide after glucagon
Item
c-peptide < 0.03 nmol/l (<0.09 µg/l) 6 min. after glucagon iv (1mg) (glycemia > 180 mg/dl)
boolean
C0202100 (UMLS CUI [1,1])
C0332282 (UMLS CUI [1,2])
C0017687 (UMLS CUI [1,3])
ebv antibody positive
Item
ebv antibody positive
boolean
C0241883 (UMLS CUI [1])
informed consent, compliance
Item
cooperative and reliable patient giving informed consent by signature; the patient should be informed in sufficient detail on the content and procedure of the protocol, indicating potential risks of intervention and of immunosuppressive therapy; the patient should also be informed that withdrawal of immunosuppressive therapy in patients with persistent plasma c-peptide positivity may result in subsequent loss of ß-cell graft function; the ß cell implant should be identified as a clinical trial.
boolean
C0021430 (UMLS CUI [1])
C1321605 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
thrombosis, pulmonary embolism
Item
history of thrombosis or pulmonary embolism
boolean
C0040053 (UMLS CUI [1])
C0034065 (UMLS CUI [2])
liver dysfunction
Item
abnormal liver function
boolean
C0086565 (UMLS CUI [1])
hla antibodies
Item
hla antibodies
boolean
C0024284 (UMLS CUI [1])

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