ID

32665

Description

Autologous Adult Stem Cells to Patients With Type 1 Diabetes and a Successful Renal Transplant; ODM derived from: https://clinicaltrials.gov/show/NCT00788827

Link

https://clinicaltrials.gov/show/NCT00788827

Keywords

Versions (1)
  1. 11/11/18 11/11/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

November 11, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Type 1 Diabetes NCT00788827

English

Eligibility Type 1 Diabetes NCT00788827

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female patients aged from 16 to 65 years of age
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patient with type i or type 2 diabetes mellitus plus:
Description

Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent

Data type

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
successful previous kidney transplant.
Description

Kidney Transplantation Successful

Data type

boolean

Alias
UMLS CUI [1,1]
C0022671
UMLS CUI [1,2]
C1272703
good kidney allograft function /no episodes of rejection for at least one year post-transplant
Description

Allograft kidney function Good | Graft rejection episode Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0564454
UMLS CUI [1,2]
C0031843
UMLS CUI [1,3]
C0205170
UMLS CUI [2,1]
C0877542
UMLS CUI [2,2]
C0332197
not taking steroids as part of standard immuno-suppression
Description

Steroids Immunosuppression Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0038317
UMLS CUI [1,2]
C0021079
UMLS CUI [1,3]
C0332197
has a who performance score of less than 2
Description

WHO performance status scale

Data type

boolean

Alias
UMLS CUI [1]
C1298650
has a life expectancy of at least 3 months
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
ability to give written consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
women of childbearing potential may be included, but must use a reliable and appropriate contraceptive method
Description

Childbearing Potential Contraceptive methods

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients below the age of 16 or above the age of 65 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients with chronic pancreatitis and poor exocrine pancreatic function
Description

Pancreatitis, Chronic | Exocrine pancreatic function test abnormal

Data type

boolean

Alias
UMLS CUI [1]
C0149521
UMLS CUI [2]
C1262139
pregnant or lactating women
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients with recent recurrent gi bleeding or spontaneous bacterial peritonitis
Description

Recurrent gastrointestinal bleeding | Spontaneous bacterial peritonitis

Data type

boolean

Alias
UMLS CUI [1]
C0585174
UMLS CUI [2]
C0275551
patients with evidence of hiv or other life threatening infection
Description

HIV Infection | Life-threatening infection

Data type

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C1859430
patients unable to give written consent
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
patients with a history of hypersensitivity to g-csf
Description

Hypersensitivity G-CSF

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0079459
patients who have been included in any other clinical trial within the previous month
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Type 1 Diabetes NCT00788827

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male or female patients aged from 16 to 65 years of age
boolean
C0001779 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
patient with type i or type 2 diabetes mellitus plus:
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
Kidney Transplantation Successful
Item
successful previous kidney transplant.
boolean
C0022671 (UMLS CUI [1,1])
C1272703 (UMLS CUI [1,2])
Allograft kidney function Good | Graft rejection episode Absent
Item
good kidney allograft function /no episodes of rejection for at least one year post-transplant
boolean
C0564454 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0205170 (UMLS CUI [1,3])
C0877542 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Steroids Immunosuppression Absent
Item
not taking steroids as part of standard immuno-suppression
boolean
C0038317 (UMLS CUI [1,1])
C0021079 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
WHO performance status scale
Item
has a who performance score of less than 2
boolean
C1298650 (UMLS CUI [1])
Life Expectancy
Item
has a life expectancy of at least 3 months
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
ability to give written consent
boolean
C0021430 (UMLS CUI [1])
Childbearing Potential Contraceptive methods
Item
women of childbearing potential may be included, but must use a reliable and appropriate contraceptive method
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Age
Item
patients below the age of 16 or above the age of 65 years
boolean
C0001779 (UMLS CUI [1])
Pancreatitis, Chronic | Exocrine pancreatic function test abnormal
Item
patients with chronic pancreatitis and poor exocrine pancreatic function
boolean
C0149521 (UMLS CUI [1])
C1262139 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Recurrent gastrointestinal bleeding | Spontaneous bacterial peritonitis
Item
patients with recent recurrent gi bleeding or spontaneous bacterial peritonitis
boolean
C0585174 (UMLS CUI [1])
C0275551 (UMLS CUI [2])
HIV Infection | Life-threatening infection
Item
patients with evidence of hiv or other life threatening infection
boolean
C0019693 (UMLS CUI [1])
C1859430 (UMLS CUI [2])
Informed Consent Unable
Item
patients unable to give written consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Hypersensitivity G-CSF
Item
patients with a history of hypersensitivity to g-csf
boolean
C0020517 (UMLS CUI [1,1])
C0079459 (UMLS CUI [1,2])
Study Subject Participation Status
Item
patients who have been included in any other clinical trial within the previous month
boolean
C2348568 (UMLS CUI [1])
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