Informations:
Erreur:
ID
22871
Description
Effects of Six Months of Moderate Resistance- Versus Endurance-Training on Muscle ATP Synthesis in First-Degree Relatives of Patients With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01145092
Lien
https://clinicaltrials.gov/show/NCT01145092
Mots-clés
Versions (1)
- 2017-06-13 2017-06-13 -
Téléchargé le
13 juni 2017
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Type 2 Diabetes Mellitus NCT01145092
Eligibility Type 2 Diabetes Mellitus NCT01145092
- StudyEvent: Eligibility
Similar models
Eligibility Type 2 Diabetes Mellitus NCT01145092
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
first degree relatives of type 2 diabetic patients
Item
first degree relatives of type 2 diabetic patients
boolean
C1517194 (UMLS CUI [1,1])
C0011860 (UMLS CUI [1,2])
C0011860 (UMLS CUI [1,2])
age
Item
age: 18-50 years
boolean
C0001779 (UMLS CUI [1])
BMI
Item
bmi <30 kg/m2 (due to limited mr diameter)
boolean
C1305855 (UMLS CUI [1])
blood cell count, kidney, liver, pancreas, thyroid and neuromuscular function
Item
normal routine lab tests (blood cell count, kidney, liver, pancreas, thyroid and neuromuscular function)
boolean
C0005771 (UMLS CUI [1])
C0232804 (UMLS CUI [2])
C0232741 (UMLS CUI [3])
C0232786 (UMLS CUI [4])
C2242456 (UMLS CUI [5])
C0597053 (UMLS CUI [6])
C0232804 (UMLS CUI [2])
C0232741 (UMLS CUI [3])
C0232786 (UMLS CUI [4])
C2242456 (UMLS CUI [5])
C0597053 (UMLS CUI [6])
availability within the local area throughout the study
Item
availability within the local area throughout the study
boolean
C0017446 (UMLS CUI [1])
informed consent
Item
ability to understand and sign the consent forms
boolean
C0021430 (UMLS CUI [1])
tobacco use
Item
current smoking
boolean
C0543414 (UMLS CUI [1])
present drug treatment
Item
present drug treatment
boolean
C0521116 (UMLS CUI [1,1])
C0013216 (UMLS CUI [1,2])
C0013216 (UMLS CUI [1,2])
regular exercise training
Item
regular exercise training
boolean
C0582191 (UMLS CUI [1])
claustrophobia, metalliferous implants
Item
contraindications for mrs studies: claustrophobia and metalliferous implants
boolean
C0008909 (UMLS CUI [1])
C3693688 (UMLS CUI [2])
C3693688 (UMLS CUI [2])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
hiv, hepatitis
Item
hiv or hepatitis
boolean
C0019682 (UMLS CUI [1])
C0019158 (UMLS CUI [2])
C0019158 (UMLS CUI [2])
acute disease
Item
acute disease 2 weeks previous to the examination
boolean
C0001314 (UMLS CUI [1])
Heart Disease
Item
heart disease
boolean
C0018799 (UMLS CUI [1])
hypertension
Item
hypertension (rr>140/95)
boolean
C0020538 (UMLS CUI [1])
liver disease
Item
liver disease
boolean
C0023895 (UMLS CUI [1])
kidney disease
Item
kidney disease
boolean
C0022658 (UMLS CUI [1])
pulmonary disease
Item
pulmonary disease
boolean
C0024115 (UMLS CUI [1])
thyroid disease
Item
thyroid disease
boolean
C0040128 (UMLS CUI [1])