ID

33647

Beschrijving

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

Trefwoorden

  1. 18-12-18 18-12-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

18 december 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus NCT01065402

Eligibility Diabetes Mellitus NCT01065402

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. diabetes mellitus patient.
Beschrijving

Diabetes Mellitus

Datatype

boolean

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

Age

Datatype

boolean

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

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

Substance Use Disorders

Datatype

boolean

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

Hypersensitivity Analog

Datatype

boolean

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

Cardiovascular Diseases Serious

Datatype

boolean

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

Study Subject Participation Status

Datatype

boolean

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

Influenza | Autoimmune Diseases | Metabolic Diseases

Datatype

boolean

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

Pregnancy | Breast Feeding

Datatype

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.
Beschrijving

Study Subject Participation Status Unfavorable

Datatype

boolean

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

Similar models

Eligibility Diabetes Mellitus NCT01065402

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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