ID

28468

Beskrivning

Study to Test the Efficacy and Safety of Drug Eluting vs. Bare-Metal Stents for Saphenous Vein Graft Interventions; ODM derived from: https://clinicaltrials.gov/show/NCT00595647

Länk

https://clinicaltrials.gov/show/NCT00595647

Nyckelord

Versioner (1)
  1. 2018-01-16 2018-01-16 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

16 januari 2018

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Coronary Artery Disease NCT00595647

Engelsk

Eligibility Coronary Artery Disease NCT00595647

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing svg pci with a target vessel reference diameter ≤ 5.5 mm (visual estimate)
Beskrivning

Saphenous vein graft | Percutaneous Coronary Intervention | Target vessel Diameter Size

Datatyp

boolean

Alias
UMLS CUI [1]
C0729538
UMLS CUI [2]
C1532338
UMLS CUI [3,1]
C0449618
UMLS CUI [3,2]
C1301886
UMLS CUI [3,3]
C0456389
documented silent ischemia, stable angina pectoris canadian cardiovascular society (ccs) class i to iv, or acute coronary syndrome
Beskrivning

Silent myocardial ischemia | Stable angina CCS Grading Scale Class | Acute Coronary Syndrome

Datatyp

boolean

Alias
UMLS CUI [1]
C0340291
UMLS CUI [2,1]
C0340288
UMLS CUI [2,2]
C1879987
UMLS CUI [3]
C0948089
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous stent implantation anywhere in the target svg
Beskrivning

Placement of stent Target Saphenous vein graft

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0522776
UMLS CUI [1,2]
C1521840
UMLS CUI [1,3]
C0729538
concomitant native vessel pci
Beskrivning

Percutaneous Coronary Intervention Vessel Native

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0005847
UMLS CUI [1,3]
C0302891
svg age <6 months
Beskrivning

Saphenous vein graft Recent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0729538
UMLS CUI [1,2]
C0332185
arterial grafts
Beskrivning

Arterial graft

Datatyp

boolean

Alias
UMLS CUI [1]
C0450140
oral anticoagulation
Beskrivning

Anticoagulation Therapy Oral

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C1527415
platelet count <100x109/l or >700x109/l, white blood cell count <3000 cells/mm3
Beskrivning

Platelet Count measurement | White Blood Cell Count procedure

Datatyp

boolean

Alias
UMLS CUI [1]
C0032181
UMLS CUI [2]
C0023508
any major non-cardiac condition with a life expectancy <12 months
Beskrivning

Medical condition Major | Exception Heart Diseases | Life Expectancy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0205164
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018799
UMLS CUI [3]
C0023671
planned elective surgery in the next 12 months
Beskrivning

Elective Surgical Procedures Planned

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0206058
UMLS CUI [1,2]
C1301732
known allergies against the components tested
Beskrivning

Hypersensitivity Investigational New Drugs

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
enrolled in other study
Beskrivning

Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
no consent
Beskrivning

Informed Consent Lacking

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268
patients unlikely to comply to the study treatment and the follow-up visits
Beskrivning

Protocol Compliance Unlikely

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0750558
age <18 years
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
known pregnancy
Beskrivning

Pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
Tillbaka till toppen

Similar models

Eligibility Coronary Artery Disease NCT00595647

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Saphenous vein graft | Percutaneous Coronary Intervention | Target vessel Diameter Size
Item
patients undergoing svg pci with a target vessel reference diameter ≤ 5.5 mm (visual estimate)
boolean
C0729538 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
C0449618 (UMLS CUI [3,1])
C1301886 (UMLS CUI [3,2])
C0456389 (UMLS CUI [3,3])
Silent myocardial ischemia | Stable angina CCS Grading Scale Class | Acute Coronary Syndrome
Item
documented silent ischemia, stable angina pectoris canadian cardiovascular society (ccs) class i to iv, or acute coronary syndrome
boolean
C0340291 (UMLS CUI [1])
C0340288 (UMLS CUI [2,1])
C1879987 (UMLS CUI [2,2])
C0948089 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Placement of stent Target Saphenous vein graft
Item
previous stent implantation anywhere in the target svg
boolean
C0522776 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C0729538 (UMLS CUI [1,3])
Percutaneous Coronary Intervention Vessel Native
Item
concomitant native vessel pci
boolean
C1532338 (UMLS CUI [1,1])
C0005847 (UMLS CUI [1,2])
C0302891 (UMLS CUI [1,3])
Saphenous vein graft Recent
Item
svg age <6 months
boolean
C0729538 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Arterial graft
Item
arterial grafts
boolean
C0450140 (UMLS CUI [1])
Anticoagulation Therapy Oral
Item
oral anticoagulation
boolean
C0003281 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
Platelet Count measurement | White Blood Cell Count procedure
Item
platelet count <100x109/l or >700x109/l, white blood cell count <3000 cells/mm3
boolean
C0032181 (UMLS CUI [1])
C0023508 (UMLS CUI [2])
Medical condition Major | Exception Heart Diseases | Life Expectancy
Item
any major non-cardiac condition with a life expectancy <12 months
boolean
C3843040 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
C0023671 (UMLS CUI [3])
Elective Surgical Procedures Planned
Item
planned elective surgery in the next 12 months
boolean
C0206058 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Hypersensitivity Investigational New Drugs
Item
known allergies against the components tested
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
Study Subject Participation Status
Item
enrolled in other study
boolean
C2348568 (UMLS CUI [1])
Informed Consent Lacking
Item
no consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Protocol Compliance Unlikely
Item
patients unlikely to comply to the study treatment and the follow-up visits
boolean
C0525058 (UMLS CUI [1,1])
C0750558 (UMLS CUI [1,2])
Age
Item
age <18 years
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
known pregnancy
boolean
C0032961 (UMLS CUI [1])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

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