Informations:
Erreur:
ID
34776
Description
Activator and Type II Diabetics; ODM derived from: https://clinicaltrials.gov/show/NCT01782092
Lien
https://clinicaltrials.gov/show/NCT01782092
Mots-clés
Versions (1)
- 28/01/2019 28/01/2019 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
28 janvier 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Eligibility Type II Diabetes NCT01782092
Eligibility Type II Diabetes NCT01782092
- StudyEvent: Eligibility
Similar models
Eligibility Type II Diabetes NCT01782092
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Age | Diabetes Mellitus, Non-Insulin-Dependent | Plasma fasting glucose measurement Quantity
Item
subjects will be eligible to participate in the study if they are between the ages of 30-60 and are clinically diagnosed with type ii diabetes by their primary care providers or endocrinologists (diagnosis usually based on fpg > 126 mg/dl on two occasions).
boolean
C0001779 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
C0583513 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0011860 (UMLS CUI [2])
C0583513 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Disease length | Medical Surveillance
Item
participants must have been diagnosed for at least one year and currently be under medical supervision for the disease.
boolean
C0872146 (UMLS CUI [1])
C0733511 (UMLS CUI [2])
C0733511 (UMLS CUI [2])
Hemoglobin A1c measurement | Disease Management Suboptimal
Item
they must also have an a1c measurement above 7%, which indicates less than optimal management of the disease.
boolean
C0474680 (UMLS CUI [1])
C0376636 (UMLS CUI [2,1])
C2984009 (UMLS CUI [2,2])
C0376636 (UMLS CUI [2,1])
C2984009 (UMLS CUI [2,2])
Pregnancy
Item
the study will exclude pregnant women;
boolean
C0032961 (UMLS CUI [1])
Comorbidity Affecting Life Expectancy | Malignant Neoplasms | Cardiovascular Diseases | Uncontrolled hypertension
Item
those with co-morbidities affecting life expectancy (e.g. malignancy, cvd); uncontrolled hypertension (> 150/100 mmhg);
boolean
C0009488 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
C1868885 (UMLS CUI [4])
C0392760 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
C1868885 (UMLS CUI [4])
Trauma Serious | Motor vehicle accident
Item
serious trauma (e.g. mva) within the previous 12 months;
boolean
C3714660 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C2939181 (UMLS CUI [2])
C0205404 (UMLS CUI [1,2])
C2939181 (UMLS CUI [2])
Blood Coagulation Disorders | Chiropractic procedure | Spinal Fracture | Communicable Disease | Arthritis | Severe osteoporosis
Item
diagnosed bleeding/clotting disorders; those currently under chiropractic care or having contraindications to activator care (e.g. vertebral fracture, infection, active inflammatory arthritis, severe osteoporosis).
boolean
C0005779 (UMLS CUI [1])
C0344217 (UMLS CUI [2])
C0080179 (UMLS CUI [3])
C0009450 (UMLS CUI [4])
C0003864 (UMLS CUI [5])
C1859443 (UMLS CUI [6])
C0344217 (UMLS CUI [2])
C0080179 (UMLS CUI [3])
C0009450 (UMLS CUI [4])
C0003864 (UMLS CUI [5])
C1859443 (UMLS CUI [6])
Gender Request for Contraceptive methods
Item
the presence of these exclusions will be determined during the history and exam procedures. all female subjects will be asked to take precautions during their participation in the study to avoid becoming pregnant.
boolean
C0079399 (UMLS CUI [1,1])
C0686900 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
C0686900 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])