ID

32628

Descripción

Cotransplantation of Islet and Mesenchymal Stem Cell in Type 1 Diabetic Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00646724

Link

https://clinicaltrials.gov/show/NCT00646724

Palabras clave

Versiones (1)
  1. 8/11/18 8/11/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

8 de noviembre de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Type 1 Diabetes Mellitus NCT00646724

Inglés

Eligibility Type 1 Diabetes Mellitus NCT00646724

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female patients age 18 to 60 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
ability to provide written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
manifest signs and symptoms that are severe enough to be incapacitating
Descripción

Signs and Symptoms Severe | Disability

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0037088
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0231170
patients with poor diabetes control (hba1c > 7% but < 12%)
Descripción

Diabetes mellitus poor control | Hemoglobin A1c measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0860161
UMLS CUI [2]
C0474680
progressive diabetic complications
Descripción

Complications of Diabetes Mellitus Progressive

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0342257
UMLS CUI [1,2]
C0205329
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < 18 years or > 60 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
diabetic history < 5 years
Descripción

Diabetes Mellitus Disease length

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0872146
bmi > 27
Descripción

Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
body weight > 80 kg
Descripción

Body Weight

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005910
exogenous insulin requirement > 1 unit/kg/day
Descripción

Requirement Insulin Exogenous U/kg/day

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1514873
UMLS CUI [1,2]
C0021641
UMLS CUI [1,3]
C0205228
UMLS CUI [1,4]
C1532634
severe anemia (male < 8 g/dl, female < 7 g/dl)
Descripción

Anemia, severe | Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0238644
UMLS CUI [2]
C0079399
low white blood cell count (< 3000/dl)
Descripción

White blood cell count decreased

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0750394
liver dysfunction
Descripción

Liver Dysfunction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0086565
active infection including hepatitis b, hepatitis c, hiv, or tb
Descripción

Communicable Disease | Hepatitis B | Hepatitis C | HIV Infection | Tuberculosis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0019163
UMLS CUI [3]
C0019196
UMLS CUI [4]
C0019693
UMLS CUI [5]
C0041296
panel reactive antibody > 20%
Descripción

Panel-reactive antibody

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1141951
any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial
Descripción

Medical condition Interferes with Completion of clinical trial

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C2732579
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Similar models

Eligibility Type 1 Diabetes Mellitus NCT00646724

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male and female patients age 18 to 60 years of age
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
ability to provide written informed consent
boolean
C0021430 (UMLS CUI [1])
Signs and Symptoms Severe | Disability
Item
manifest signs and symptoms that are severe enough to be incapacitating
boolean
C0037088 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0231170 (UMLS CUI [2])
Diabetes mellitus poor control | Hemoglobin A1c measurement
Item
patients with poor diabetes control (hba1c > 7% but < 12%)
boolean
C0860161 (UMLS CUI [1])
C0474680 (UMLS CUI [2])
Complications of Diabetes Mellitus Progressive
Item
progressive diabetic complications
boolean
C0342257 (UMLS CUI [1,1])
C0205329 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Age
Item
age < 18 years or > 60 years
boolean
C0001779 (UMLS CUI [1])
Diabetes Mellitus Disease length
Item
diabetic history < 5 years
boolean
C0011849 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Body mass index
Item
bmi > 27
boolean
C1305855 (UMLS CUI [1])
Body Weight
Item
body weight > 80 kg
boolean
C0005910 (UMLS CUI [1])
Requirement Insulin Exogenous U/kg/day
Item
exogenous insulin requirement > 1 unit/kg/day
boolean
C1514873 (UMLS CUI [1,1])
C0021641 (UMLS CUI [1,2])
C0205228 (UMLS CUI [1,3])
C1532634 (UMLS CUI [1,4])
Anemia, severe | Gender
Item
severe anemia (male < 8 g/dl, female < 7 g/dl)
boolean
C0238644 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
White blood cell count decreased
Item
low white blood cell count (< 3000/dl)
boolean
C0750394 (UMLS CUI [1])
Liver Dysfunction
Item
liver dysfunction
boolean
C0086565 (UMLS CUI [1])
Communicable Disease | Hepatitis B | Hepatitis C | HIV Infection | Tuberculosis
Item
active infection including hepatitis b, hepatitis c, hiv, or tb
boolean
C0009450 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
C0019693 (UMLS CUI [4])
C0041296 (UMLS CUI [5])
Panel-reactive antibody
Item
panel reactive antibody > 20%
boolean
C1141951 (UMLS CUI [1])
Medical condition Interferes with Completion of clinical trial
Item
any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial
boolean
C3843040 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2732579 (UMLS CUI [1,3])
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