Informations:
Erreur:
ID
24468
Description
Safe Renal Function In Long Term Heart Transplanted Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00505102
Lien
https://clinicaltrials.gov/show/NCT00505102
Mots-clés
Versions (1)
- 02/08/2017 02/08/2017 -
Téléchargé le
2 août 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 Kidney Diseases NCT00505102
Eligibility Kidney Diseases NCT00505102
- StudyEvent: Eligibility
Similar models
Eligibility Kidney Diseases NCT00505102
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Heart Transplantation | Follow-up Duration
Item
heart transplant patients with more than 1 year of follow-up
boolean
C0018823 (UMLS CUI [1])
C3274571 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C3274571 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Creatinine measurement, serum
Item
creatinine lower than 3.5 mg/dl
boolean
C0201976 (UMLS CUI [1])
Glomerular Filtration Rate Cockcroft-Gault formula
Item
gfr higher than 20 ml/min (calculated with cockcroft-gault formula)
boolean
C0017654 (UMLS CUI [1,1])
C2924627 (UMLS CUI [1,2])
C2924627 (UMLS CUI [1,2])
Cyclosporine | Therapeutic immunosuppression
Item
cyclosporine in maintenance immunosuppressive therapy
boolean
C0010592 (UMLS CUI [1])
C0021079 (UMLS CUI [2])
C0021079 (UMLS CUI [2])
Informed Consent
Item
patient must be able to sign an approve informed consent
boolean
C0021430 (UMLS CUI [1])
Graft Rejection Within Period
Item
prior history of acute rejection within the last 3 months
boolean
C0018129 (UMLS CUI [1,1])
C0332285 (UMLS CUI [1,2])
C1948053 (UMLS CUI [1,3])
C0332285 (UMLS CUI [1,2])
C1948053 (UMLS CUI [1,3])
Childbearing Potential Pregnancy Excluded | Childbearing Potential Contraceptive methods
Item
females of childbearing age may be included if pregnancy is excluded and acceptable contraception measures are used
boolean
C3831118 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0032961 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
Recipient Organ transplant multiple
Item
patients who are recipients of multiple organ transplants
boolean
C1709854 (UMLS CUI [1,1])
C0524930 (UMLS CUI [1,2])
C0439064 (UMLS CUI [1,3])
C0524930 (UMLS CUI [1,2])
C0439064 (UMLS CUI [1,3])
Sirolimus | Everolimus
Item
prior or current use of sirolimus or everolimus
boolean
C0072980 (UMLS CUI [1])
C0541315 (UMLS CUI [2])
C0541315 (UMLS CUI [2])
Graft Rejection Within Period
Item
history of acute rejection within the last 6 months
boolean
C0018129 (UMLS CUI [1,1])
C0332285 (UMLS CUI [1,2])
C1948053 (UMLS CUI [1,3])
C0332285 (UMLS CUI [1,2])
C1948053 (UMLS CUI [1,3])
Coronary Artery Bypass Surgery | Cardiac Surgery
Item
coronary artery bypass surgery or other cardiac surgery in the past 3 months
boolean
C0010055 (UMLS CUI [1])
C0018821 (UMLS CUI [2])
C0018821 (UMLS CUI [2])
Patient Unavailable Follow-up Evaluation
Item
patient not able to attend all follow-up evaluations
boolean
C0030705 (UMLS CUI [1,1])
C0686905 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
C0220825 (UMLS CUI [1,4])
C0686905 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
C0220825 (UMLS CUI [1,4])