ID

41027

Description

A Prospective, Single Arm, Multi-Center Clinical Study in Collaboration With the Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS®) to Evaluate the Thoracotomy Implant Technique of the HeartWare HVAD® System in Patients With Advanced Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT02268942

Lien

https://clinicaltrials.gov/show/NCT02268942

Mots-clés

Versions (1)
  1. 15/06/2020 15/06/2020 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

15 juin 2020

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Left Sided Heart Failure NCT02268942

Anglais

Eligibility Left Sided Heart Failure NCT02268942

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. must be ≥19 years of age at time of informed consent to participate in the intermacs®
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
registry.
Description

ID.2

Type de données

boolean

2. subject receives a heartware® hvad (the device should be the subject's first vad implant).
Description

Ventricular Assist Device Placement Firstly

Type de données

boolean

Alias
UMLS CUI [1,1]
C2825193
UMLS CUI [1,2]
C1279901
3. subject signed an intermacs® informed consent if required by local irb policy.
Description

Informed Consent Specified

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0205369
4. subject signed a heartware ®informed consent.
Description

Informed Consent Specified

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0205369
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. subject is incarcerated (prisoner).
Description

Prisoner

Type de données

boolean

Alias
UMLS CUI [1]
C0033167
2. subject did not sign the informed consent at sites where waiver of consent was not granted.
Description

Informed Consent Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332197
3. body surface area (bsa) < 1.2 m^2.
Description

Body Surface Area

Type de données

boolean

Alias
UMLS CUI [1]
C0005902
4. prior cardiac transplant or cardiomyoplasty.
Description

Heart Transplantation | Cardiomyopathy

Type de données

boolean

Alias
UMLS CUI [1]
C0018823
UMLS CUI [2]
C0878544
5. subject is receiving a bivad.
Description

Implantation of biventricular assist device

Type de données

boolean

Alias
UMLS CUI [1]
C0397131
6. subject is receiving the device as an rvad.
Description

Right Cardiac Ventricle Assist Device Procedure

Type de données

boolean

Alias
UMLS CUI [1]
C3272255
7. subject data is generated from non- intermacs® centers.
Description

Patient data Clinic/Center Other

Type de données

boolean

Alias
UMLS CUI [1,1]
C2707520
UMLS CUI [1,2]
C1552416
UMLS CUI [1,3]
C0205394
8. pediatric subjects (< 19 years of age).
Description

Study Subject Pediatric | Age

Type de données

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C1521725
UMLS CUI [2]
C0001779
9. subjects who receive a temporary lvad
Description

Implantation of left ventricular assist device temporary

Type de données

boolean

Alias
UMLS CUI [1,1]
C0397130
UMLS CUI [1,2]
C0205374
10. subjects whose device strategy is listed as "destination therapy" at the time of implant.
Description

Device strategy specified

Type de données

boolean

Alias
UMLS CUI [1,1]
C0085842
UMLS CUI [1,2]
C0679199
UMLS CUI [1,3]
C0205369
11. severe right heart failure
Description

Right-Sided Heart Failure Severe

Type de données

boolean

Alias
UMLS CUI [1,1]
C0235527
UMLS CUI [1,2]
C0205082
12. aortic insufficiency or mechanical aortic valve.
Description

Aortic Valve Insufficiency | Mechanical Aortic Valve

Type de données

boolean

Alias
UMLS CUI [1]
C0003504
UMLS CUI [2]
C2825203
13. planned concomitant procedure (e.g.valve repair or replacement, cabg, septal defect repair).
Description

Planned procedure | Repair of heart valve | Valve replacement | Coronary Artery Bypass Surgery | Repair Procedures for Septal Defect

Type de données

boolean

Alias
UMLS CUI [1]
C1320712
UMLS CUI [2]
C0190112
UMLS CUI [3]
C1410969
UMLS CUI [4]
C0010055
UMLS CUI [5]
C0519387
14. known lv thrombus.
Description

Left ventricular thrombus

Type de données

boolean

Alias
UMLS CUI [1]
C0587044
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Similar models

Eligibility Left Sided Heart Failure NCT02268942

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1. must be ≥19 years of age at time of informed consent to participate in the intermacs®
boolean
C0001779 (UMLS CUI [1])
ID.2
Item
registry.
boolean
Ventricular Assist Device Placement Firstly
Item
2. subject receives a heartware® hvad (the device should be the subject's first vad implant).
boolean
C2825193 (UMLS CUI [1,1])
C1279901 (UMLS CUI [1,2])
Informed Consent Specified
Item
3. subject signed an intermacs® informed consent if required by local irb policy.
boolean
C0021430 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
Informed Consent Specified
Item
4. subject signed a heartware ®informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Prisoner
Item
1. subject is incarcerated (prisoner).
boolean
C0033167 (UMLS CUI [1])
Informed Consent Absent
Item
2. subject did not sign the informed consent at sites where waiver of consent was not granted.
boolean
C0021430 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Body Surface Area
Item
3. body surface area (bsa) < 1.2 m^2.
boolean
C0005902 (UMLS CUI [1])
Heart Transplantation | Cardiomyopathy
Item
4. prior cardiac transplant or cardiomyoplasty.
boolean
C0018823 (UMLS CUI [1])
C0878544 (UMLS CUI [2])
Implantation of biventricular assist device
Item
5. subject is receiving a bivad.
boolean
C0397131 (UMLS CUI [1])
Right Cardiac Ventricle Assist Device Procedure
Item
6. subject is receiving the device as an rvad.
boolean
C3272255 (UMLS CUI [1])
Patient data Clinic/Center Other
Item
7. subject data is generated from non- intermacs® centers.
boolean
C2707520 (UMLS CUI [1,1])
C1552416 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Study Subject Pediatric | Age
Item
8. pediatric subjects (< 19 years of age).
boolean
C0681850 (UMLS CUI [1,1])
C1521725 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Implantation of left ventricular assist device temporary
Item
9. subjects who receive a temporary lvad
boolean
C0397130 (UMLS CUI [1,1])
C0205374 (UMLS CUI [1,2])
Device strategy specified
Item
10. subjects whose device strategy is listed as "destination therapy" at the time of implant.
boolean
C0085842 (UMLS CUI [1,1])
C0679199 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Right-Sided Heart Failure Severe
Item
11. severe right heart failure
boolean
C0235527 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Aortic Valve Insufficiency | Mechanical Aortic Valve
Item
12. aortic insufficiency or mechanical aortic valve.
boolean
C0003504 (UMLS CUI [1])
C2825203 (UMLS CUI [2])
Planned procedure | Repair of heart valve | Valve replacement | Coronary Artery Bypass Surgery | Repair Procedures for Septal Defect
Item
13. planned concomitant procedure (e.g.valve repair or replacement, cabg, septal defect repair).
boolean
C1320712 (UMLS CUI [1])
C0190112 (UMLS CUI [2])
C1410969 (UMLS CUI [3])
C0010055 (UMLS CUI [4])
C0519387 (UMLS CUI [5])
Left ventricular thrombus
Item
14. known lv thrombus.
boolean
C0587044 (UMLS CUI [1])
Retour au début de la page 

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