Informations:
Erreur:
ID
23914
Description
Coronary Artery and Coronary Artery Bypass Graft Imaging Using a Specialized Catheter and Computed Tomography; ODM derived from: https://clinicaltrials.gov/show/NCT00474565
Lien
https://clinicaltrials.gov/show/NCT00474565
Mots-clés
Versions (1)
- 17/07/2017 17/07/2017 -
Téléchargé le
17 juillet 2017
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 Coronary Artery Disease NCT00474565
Eligibility Coronary Artery Disease NCT00474565
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease NCT00474565
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Heart Radionuclide Imaging Abnormal | Cardiac Catheterization Scheduled | Coronary Artery Disease Evaluation | Coronary Artery Bypass Surgery
Item
1. male and female patients that have an abnormal nuclear medicine heart scan and are already scheduled for cardiac catheterization for evaluation of coronary artery disease or disease of coronary artery bypass grafts will be asked to participate in this trial.
boolean
C0018787 (UMLS CUI [1,1])
C0034606 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,3])
C0018795 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
C1956346 (UMLS CUI [3,1])
C1261322 (UMLS CUI [3,2])
C0010055 (UMLS CUI [4])
C0034606 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,3])
C0018795 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
C1956346 (UMLS CUI [3,1])
C1261322 (UMLS CUI [3,2])
C0010055 (UMLS CUI [4])
Informed Consent
Item
2. provided informed consent.
boolean
C0021430 (UMLS CUI [1])
Evaluation
Item
3. evaluation by a cardiology division staff or cardiology nurse clinician.
boolean
C0220825 (UMLS CUI [1])
Study Subject Participation Status | Research study Related
Item
1. patient is currently enrolled in another related research study.
boolean
C2348568 (UMLS CUI [1])
C0681814 (UMLS CUI [2,1])
C0439849 (UMLS CUI [2,2])
C0681814 (UMLS CUI [2,1])
C0439849 (UMLS CUI [2,2])
Age
Item
2. less than 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
3. pregnant patients.
boolean
C0032961 (UMLS CUI [1])
Abnormal renal function | Creatinine measurement, serum | Dialysis Patient need for
Item
4. abnormal renal function with creatinine equal to or greater than 1.6 mg/dl or those subjects requiring dialysis.
boolean
C0151746 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0011946 (UMLS CUI [3,1])
C0686904 (UMLS CUI [3,2])
C0201976 (UMLS CUI [2])
C0011946 (UMLS CUI [3,1])
C0686904 (UMLS CUI [3,2])
Chronic Obstructive Airway Disease | Heart failure | Cardiac ejection fraction
Item
5. patients with chronic obstructive pulmonary disease or heart-failure with cardiac ejection-fraction less than 30%.
boolean
C0024117 (UMLS CUI [1])
C0018801 (UMLS CUI [2])
C0232174 (UMLS CUI [3])
C0018801 (UMLS CUI [2])
C0232174 (UMLS CUI [3])
Hypersensitivity Adrenergic beta-Antagonists | Hypersensitivity Lopressor | Asthma
Item
6. patients with known sensitivity to beta-blockers (lopressor) or have asthma.
boolean
C0020517 (UMLS CUI [1,1])
C0001645 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0700776 (UMLS CUI [2,2])
C0004096 (UMLS CUI [3])
C0001645 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0700776 (UMLS CUI [2,2])
C0004096 (UMLS CUI [3])
Contrast Media Large Abnormal | Cardiac Catheterization
Item
7. patients receiving an abnormally large volume of contrast media during cardiac catheterization (> 200cc)
boolean
C0009924 (UMLS CUI [1,1])
C0549177 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,3])
C0018795 (UMLS CUI [2])
C0549177 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,3])
C0018795 (UMLS CUI [2])