ID

30114

Description

Reduction or Discontinuation of CNI's With Conversion to Everolimus-Based Immunosuppresion; ODM derived from: https://clinicaltrials.gov/show/NCT00443508

Lien

https://clinicaltrials.gov/show/NCT00443508

Mots-clés

  1. 12/05/2018 12/05/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

12 mai 2018

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 NCT00443508

Eligibility Kidney Diseases NCT00443508

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients on cni fk < 5 ng/m"l with mpa / imuran with or without steroids
Description

Calcineurin inhibitor | Tacrolimus | Mycophenolic Acid | Imuran | Steroids

Type de données

boolean

Alias
UMLS CUI [1]
C1562036
UMLS CUI [2]
C0085149
UMLS CUI [3]
C0026933
UMLS CUI [4]
C0699279
UMLS CUI [5]
C0038317
renal impairment gfr between 30 - 70 m"l/minute/
Description

Renal Insufficiency | Glomerular Filtration Rate

Type de données

boolean

Alias
UMLS CUI [1]
C1565489
UMLS CUI [2]
C0017654
patient who signed informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
patient with no contraindication to renal biopsy
Description

Medical contraindication Absent Kidney biopsy

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0194073
women who are not pregnant and will use contraception
Description

Gender Pregnancy Absent | Gender Contraceptive methods

Type de données

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0032961
UMLS CUI [1,3]
C0332197
UMLS CUI [2,1]
C0079399
UMLS CUI [2,2]
C0700589
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
proteinuria > 100 m"g/mmol creatinine
Description

Proteinuria | Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1]
C0033687
UMLS CUI [2]
C0201976
acute rejection during 3 months before screening
Description

Graft Rejection

Type de données

boolean

Alias
UMLS CUI [1]
C0018129
wbc < 2500, plt < 50,000,
Description

White Blood Cell Count procedure | Platelet Count measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0032181
nephropathy due to polyoma virus
Description

Kidney Disease Due to Polyomavirus

Type de données

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0032556
patients on other investigational drugs
Description

Investigational New Drugs

Type de données

boolean

Alias
UMLS CUI [1]
C0013230
patients on rapamycin
Description

Sirolimus

Type de données

boolean

Alias
UMLS CUI [1]
C0072980
patients with hiv or other systemic infection
Description

HIV Infections | Sepsis

Type de données

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0243026
inability to comply with protocol requirements
Description

Protocol Compliance Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
active or history of malignancy
Description

Malignant Neoplasms

Type de données

boolean

Alias
UMLS CUI [1]
C0006826

Similar models

Eligibility Kidney Diseases NCT00443508

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Calcineurin inhibitor | Tacrolimus | Mycophenolic Acid | Imuran | Steroids
Item
patients on cni fk < 5 ng/m"l with mpa / imuran with or without steroids
boolean
C1562036 (UMLS CUI [1])
C0085149 (UMLS CUI [2])
C0026933 (UMLS CUI [3])
C0699279 (UMLS CUI [4])
C0038317 (UMLS CUI [5])
Renal Insufficiency | Glomerular Filtration Rate
Item
renal impairment gfr between 30 - 70 m"l/minute/
boolean
C1565489 (UMLS CUI [1])
C0017654 (UMLS CUI [2])
Informed Consent
Item
patient who signed informed consent
boolean
C0021430 (UMLS CUI [1])
Medical contraindication Absent Kidney biopsy
Item
patient with no contraindication to renal biopsy
boolean
C1301624 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0194073 (UMLS CUI [1,3])
Gender Pregnancy Absent | Gender Contraceptive methods
Item
women who are not pregnant and will use contraception
boolean
C0079399 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0079399 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Proteinuria | Creatinine measurement, serum
Item
proteinuria > 100 m"g/mmol creatinine
boolean
C0033687 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Graft Rejection
Item
acute rejection during 3 months before screening
boolean
C0018129 (UMLS CUI [1])
White Blood Cell Count procedure | Platelet Count measurement
Item
wbc < 2500, plt < 50,000,
boolean
C0023508 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
Kidney Disease Due to Polyomavirus
Item
nephropathy due to polyoma virus
boolean
C0022658 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0032556 (UMLS CUI [1,3])
Investigational New Drugs
Item
patients on other investigational drugs
boolean
C0013230 (UMLS CUI [1])
Sirolimus
Item
patients on rapamycin
boolean
C0072980 (UMLS CUI [1])
HIV Infections | Sepsis
Item
patients with hiv or other systemic infection
boolean
C0019693 (UMLS CUI [1])
C0243026 (UMLS CUI [2])
Protocol Compliance Unable
Item
inability to comply with protocol requirements
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Malignant Neoplasms
Item
active or history of malignancy
boolean
C0006826 (UMLS CUI [1])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial