ID

33647

Descripción

A Study to Evaluate the Efficacy and Safety of PPB-R-203-Based Meal Versus TK9-Based Meal in 20 Patients With Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01065402

Link

https://clinicaltrials.gov/show/NCT01065402

Palabras clave

  1. 18/12/18 18/12/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

18 de diciembre de 2018

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus NCT01065402

Eligibility Diabetes Mellitus NCT01065402

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. diabetes mellitus patient.
Descripción

Diabetes Mellitus

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011849
2. aged between 20 to 65 years old.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
3. informed consent form signed.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. a recent history of drug or alcohol abuse.
Descripción

Substance Use Disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038586
2. sensitivity to analogous product.
Descripción

Hypersensitivity Analog

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0243071
3. serious cardiovascular disorders.
Descripción

Cardiovascular Diseases Serious

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0205404
4. participation in another clinical investigation study.
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
5. ongoing influenza, autoimmune disease and other metabolic diseases.
Descripción

Influenza | Autoimmune Diseases | Metabolic Diseases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021400
UMLS CUI [2]
C0004364
UMLS CUI [3]
C0025517
6. pregnant or lactating women.
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
7. individuals are judged by the investigators or co-investigator to be undesirable as subjects.
Descripción

Study Subject Participation Status Unfavorable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C3640815

Similar models

Eligibility Diabetes Mellitus NCT01065402

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus
Item
1. diabetes mellitus patient.
boolean
C0011849 (UMLS CUI [1])
Age
Item
2. aged between 20 to 65 years old.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
3. informed consent form signed.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Substance Use Disorders
Item
1. a recent history of drug or alcohol abuse.
boolean
C0038586 (UMLS CUI [1])
Hypersensitivity Analog
Item
2. sensitivity to analogous product.
boolean
C0020517 (UMLS CUI [1,1])
C0243071 (UMLS CUI [1,2])
Cardiovascular Diseases Serious
Item
3. serious cardiovascular disorders.
boolean
C0007222 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Study Subject Participation Status
Item
4. participation in another clinical investigation study.
boolean
C2348568 (UMLS CUI [1])
Influenza | Autoimmune Diseases | Metabolic Diseases
Item
5. ongoing influenza, autoimmune disease and other metabolic diseases.
boolean
C0021400 (UMLS CUI [1])
C0004364 (UMLS CUI [2])
C0025517 (UMLS CUI [3])
Pregnancy | Breast Feeding
Item
6. pregnant or lactating women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status Unfavorable
Item
7. individuals are judged by the investigators or co-investigator to be undesirable as subjects.
boolean
C2348568 (UMLS CUI [1,1])
C3640815 (UMLS CUI [1,2])

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