ID

33614

Beschrijving

Relation Among Shear Stress Distribution, Stent Design, and Subsequent Vessel Healing After Drug-eluting Stent Implantation (SHEAR DES); ODM derived from: https://clinicaltrials.gov/show/NCT01942044

Link

https://clinicaltrials.gov/show/NCT01942044

Trefwoorden

  1. 16-12-18 16-12-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

16 december 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Coronary Heart Disease NCT01942044

Eligibility Coronary Heart Disease NCT01942044

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
older than 20 years old.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
indication of pci with xience prime, nobori, or promus element.
Beschrijving

Indication Percutaneous Coronary Intervention | Other Coding

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1532338
UMLS CUI [2]
C3846158
clinical diagnosis of stable angina, unstable angina or silent ischemia with reference vessel diameters ranging from 2.5-3.5mm.
Beschrijving

Stable angina | Angina, Unstable | Silent myocardial ischemia | Reference Vessel Diameter

Datatype

boolean

Alias
UMLS CUI [1]
C0340288
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0340291
UMLS CUI [4,1]
C1706462
UMLS CUI [4,2]
C0005847
UMLS CUI [4,3]
C1301886
underwent ct angiography before pci.
Beschrijving

CT Angiography | Status pre- Percutaneous Coronary Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C1536105
UMLS CUI [2,1]
C0332152
UMLS CUI [2,2]
C1532338
to agree to review and record all the clinical course in this research protocol.
Beschrijving

Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous history of pancytopenia, liver function, renal dysfunction, hypersensitive history of the drug.
Beschrijving

Pancytopenia | Liver function | Renal dysfunction | Hypersensitivity Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C0030312
UMLS CUI [2]
C0232741
UMLS CUI [3]
C3279454
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C0013230
low ejection fraction (lvef<=30%), an impaired liver function, and renal dysfunction (egfr<=40)
Beschrijving

Left ventricular ejection fraction low | Liver Dysfunction | Renal dysfunction | Estimated Glomerular Filtration Rate

Datatype

boolean

Alias
UMLS CUI [1,1]
C0428772
UMLS CUI [1,2]
C0205251
UMLS CUI [2]
C0086565
UMLS CUI [3]
C3279454
UMLS CUI [4]
C3811844
severe calcification
Beschrijving

Calcification Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0006660
UMLS CUI [1,2]
C0205082
stent restenosis
Beschrijving

Stent restenosis

Datatype

boolean

Alias
UMLS CUI [1]
C3272317

Similar models

Eligibility Coronary Heart Disease NCT01942044

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
older than 20 years old.
boolean
C0001779 (UMLS CUI [1])
Indication Percutaneous Coronary Intervention | Other Coding
Item
indication of pci with xience prime, nobori, or promus element.
boolean
C3146298 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
C3846158 (UMLS CUI [2])
Stable angina | Angina, Unstable | Silent myocardial ischemia | Reference Vessel Diameter
Item
clinical diagnosis of stable angina, unstable angina or silent ischemia with reference vessel diameters ranging from 2.5-3.5mm.
boolean
C0340288 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0340291 (UMLS CUI [3])
C1706462 (UMLS CUI [4,1])
C0005847 (UMLS CUI [4,2])
C1301886 (UMLS CUI [4,3])
CT Angiography | Status pre- Percutaneous Coronary Intervention
Item
underwent ct angiography before pci.
boolean
C1536105 (UMLS CUI [1])
C0332152 (UMLS CUI [2,1])
C1532338 (UMLS CUI [2,2])
Protocol Compliance
Item
to agree to review and record all the clinical course in this research protocol.
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pancytopenia | Liver function | Renal dysfunction | Hypersensitivity Investigational New Drugs
Item
previous history of pancytopenia, liver function, renal dysfunction, hypersensitive history of the drug.
boolean
C0030312 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C3279454 (UMLS CUI [3])
C0020517 (UMLS CUI [4,1])
C0013230 (UMLS CUI [4,2])
Left ventricular ejection fraction low | Liver Dysfunction | Renal dysfunction | Estimated Glomerular Filtration Rate
Item
low ejection fraction (lvef<=30%), an impaired liver function, and renal dysfunction (egfr<=40)
boolean
C0428772 (UMLS CUI [1,1])
C0205251 (UMLS CUI [1,2])
C0086565 (UMLS CUI [2])
C3279454 (UMLS CUI [3])
C3811844 (UMLS CUI [4])
Calcification Severe
Item
severe calcification
boolean
C0006660 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Stent restenosis
Item
stent restenosis
boolean
C3272317 (UMLS CUI [1])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

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