ID

20506

Description

COmbined N-acetylcysteine and Bicarbonate in PCI To Reduce Adverse Side Effect of contrasT; ODM derived from: https://clinicaltrials.gov/show/NCT00497328

Lien

https://clinicaltrials.gov/show/NCT00497328

Mots-clés

Versions (1)
  1. 28/02/2017 28/02/2017 -
Téléchargé le

28 février 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.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Contrast Induced Nephropathy NCT00497328

Anglais

Eligibility Contrast Induced Nephropathy NCT00497328

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age > 21 year
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
glomerular filtration rate (gfr) 15-60ml/min calculated by mdrd formula
Description

gfr

Type de données

boolean

Alias
UMLS CUI [1]
C0017654
scheduled to undergo elective pci
Description

scheduled to undergo elective pci

Type de données

boolean

Alias
UMLS CUI [1,1]
C0439608
UMLS CUI [1,2]
C1532338
able to receive 12 hours of pre-hydration
Description

able to receive 12 hours of pre-hydration

Type de données

boolean

Alias
UMLS CUI [1]
C2034482
written informed consent
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
gfr less than 15ml/min or patients diagnosed with end stage renal failure
Description

gfr, end stage renal failure

Type de données

boolean

Alias
UMLS CUI [1,1]
C0017654
UMLS CUI [1,2]
C0022661
increase in serum creatinine levels of > 0.5mg/dl or 44umol/l in the previous 24 hours
Description

creatinine

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
preexisting dialysis
Description

dialysis

Type de données

boolean

Alias
UMLS CUI [1]
C0011946
pulmonary edema or moderate to severe congestive heart failure (new york heart association [nyha] iii-iv)
Description

pulmonary edema, congestive heart failure

Type de données

boolean

Alias
UMLS CUI [1]
C0034063
UMLS CUI [2,1]
C0018802
UMLS CUI [2,2]
C1275491
patient unable to withstand the fluid load and hemodynamics compromise
Description

Fluid Therapy; Hemodynamic regulation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0016286
UMLS CUI [1,2]
C0150249
uncontrolled hypertension (untreated systolic blood pressure > 160 mmhg, or diastolic blood pressure > 100mmhg.)
Description

uncontrolled hypertension

Type de données

boolean

Alias
UMLS CUI [1]
C1868885
emergency cardiac catheterization (i.e. patient presenting with st segment elevation myocardial infarction undergoing primary angioplasty)
Description

emergency cardiac catheterization

Type de données

boolean

Alias
UMLS CUI [1]
C1532297
recent exposure to radiographic contrast (within two days of the study).
Description

recent exposure to radiographic contrast

Type de données

boolean

Alias
UMLS CUI [1,1]
C2220266
UMLS CUI [1,2]
C0009924
allergic to radio-contrast
Description

allergic to radio-contrast

Type de données

boolean

Alias
UMLS CUI [1]
C0570562
administration of sodium bicarbonate solution or nac within 48 hours before the pci.
Description

sodium bicarbonate solution or nac before pci

Type de données

boolean

Alias
UMLS CUI [1,1]
C1247967
UMLS CUI [1,2]
C2034490
UMLS CUI [2]
C1532338
patient unable to give consent
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
clinically vulnerable condition requiring continuous fluid therapy e.g. severe sepsis
Description

Acute Disease | Continuous; Fluid Therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0001314
UMLS CUI [2,1]
C0549178
UMLS CUI [2,2]
C0016286
use of nsaid, aminoglycocide, cyclosporin, cysplatin within 48 hours prior to pci and throughout the study duration
Description

Use of; Anti-Inflammatory Agents, Non-Steroidal; Aminoglycosides; Cyclosporine; Cisplatin | Percutaneous Coronary Intervention

Type de données

boolean

Alias
UMLS CUI [1,1]
C1524063
UMLS CUI [1,2]
C0003211
UMLS CUI [1,3]
C0002556
UMLS CUI [1,4]
C0010592
UMLS CUI [1,5]
C0008838
UMLS CUI [2]
C1532338
Retour au début de la page

Similar models

Eligibility Contrast Induced Nephropathy NCT00497328

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
age > 21 year
boolean
C0001779 (UMLS CUI [1])
gfr
Item
glomerular filtration rate (gfr) 15-60ml/min calculated by mdrd formula
boolean
C0017654 (UMLS CUI [1])
scheduled to undergo elective pci
Item
scheduled to undergo elective pci
boolean
C0439608 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
able to receive 12 hours of pre-hydration
Item
able to receive 12 hours of pre-hydration
boolean
C2034482 (UMLS CUI [1])
informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
gfr, end stage renal failure
Item
gfr less than 15ml/min or patients diagnosed with end stage renal failure
boolean
C0017654 (UMLS CUI [1,1])
C0022661 (UMLS CUI [1,2])
creatinine
Item
increase in serum creatinine levels of > 0.5mg/dl or 44umol/l in the previous 24 hours
boolean
C0201976 (UMLS CUI [1])
dialysis
Item
preexisting dialysis
boolean
C0011946 (UMLS CUI [1])
pulmonary edema, congestive heart failure
Item
pulmonary edema or moderate to severe congestive heart failure (new york heart association [nyha] iii-iv)
boolean
C0034063 (UMLS CUI [1])
C0018802 (UMLS CUI [2,1])
C1275491 (UMLS CUI [2,2])
Fluid Therapy; Hemodynamic regulation
Item
patient unable to withstand the fluid load and hemodynamics compromise
boolean
C0016286 (UMLS CUI [1,1])
C0150249 (UMLS CUI [1,2])
uncontrolled hypertension
Item
uncontrolled hypertension (untreated systolic blood pressure > 160 mmhg, or diastolic blood pressure > 100mmhg.)
boolean
C1868885 (UMLS CUI [1])
emergency cardiac catheterization
Item
emergency cardiac catheterization (i.e. patient presenting with st segment elevation myocardial infarction undergoing primary angioplasty)
boolean
C1532297 (UMLS CUI [1])
recent exposure to radiographic contrast
Item
recent exposure to radiographic contrast (within two days of the study).
boolean
C2220266 (UMLS CUI [1,1])
C0009924 (UMLS CUI [1,2])
allergic to radio-contrast
Item
allergic to radio-contrast
boolean
C0570562 (UMLS CUI [1])
sodium bicarbonate solution or nac before pci
Item
administration of sodium bicarbonate solution or nac within 48 hours before the pci.
boolean
C1247967 (UMLS CUI [1,1])
C2034490 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2])
informed consent
Item
patient unable to give consent
boolean
C0021430 (UMLS CUI [1])
Acute Disease | Continuous; Fluid Therapy
Item
clinically vulnerable condition requiring continuous fluid therapy e.g. severe sepsis
boolean
C0001314 (UMLS CUI [1])
C0549178 (UMLS CUI [2,1])
C0016286 (UMLS CUI [2,2])
Use of; Anti-Inflammatory Agents, Non-Steroidal; Aminoglycosides; Cyclosporine; Cisplatin | Percutaneous Coronary Intervention
Item
use of nsaid, aminoglycocide, cyclosporin, cysplatin within 48 hours prior to pci and throughout the study duration
boolean
C1524063 (UMLS CUI [1,1])
C0003211 (UMLS CUI [1,2])
C0002556 (UMLS CUI [1,3])
C0010592 (UMLS CUI [1,4])
C0008838 (UMLS CUI [1,5])
C1532338 (UMLS CUI [2])
Retour au début de la page 

Contact

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

Les champs marqués d’un * sont obligatoires.

Aide

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