ID

19371

Beschrijving

SAVEPACe - Search AV Extension and Managed Ventricular Pacing for Promoting Atrio-Ventricular Conduction; ODM derived from: https://clinicaltrials.gov/show/NCT00284830

Link

https://clinicaltrials.gov/show/NCT00284830

Trefwoorden

Versies (1)
  1. 22-12-16 22-12-16 -
Geüploaded op

22 december 2016

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.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

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

Eligibility Sick Sinus Syndrome NCT00284830

Engels

Eligibility Sick Sinus Syndrome NCT00284830

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
18 years of age and older
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
willing and able to give informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
willing and able to comply with the study follow-up schedule
Beschrijving

Clinical Study Follow-up Compliance behavior

Datatype

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1321605
class i/classii indications for dual chamber pacing
Beschrijving

Indication Dual Chamber Pacemaker Class

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C2911683
UMLS CUI [1,3]
C3272276
initial implant of a kappa 700, kappa 900, enpulse, or enrhythm dual chamber ipg
Beschrijving

DUAL CHAMBER IMPLANTABLE PULSE-GENERATOR Implantation Initial

Datatype

boolean

Alias
UMLS CUI [1,1]
C0493526
UMLS CUI [1,2]
C0021107
UMLS CUI [1,3]
C0205265
demonstrate 1 to 1 conduction and a qrs interval of < 120ms at 100 beats per minutes for a period of nine seconds while atrial pacing
Beschrijving

1:1 atrioventricular conduction | QRS interval | Intra-atrial pacing

Datatype

boolean

Alias
UMLS CUI [1]
C2215915
UMLS CUI [2]
C2168881
UMLS CUI [3]
C0199647
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
less than 18 years of age
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
unwilling or unable to give informed consent
Beschrijving

Informed Consent Unable | Informed Consent Unwilling

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080
unwilling or unable to commit to follow-up schedule
Beschrijving

Clinical Study Follow-up Compliance behavior Lacking

Datatype

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1321605
UMLS CUI [1,3]
C0332268
medical conditions that would preclude the testing required by the protocol or limit study participation
Beschrijving

Medical condition Excludes Testing | Medical condition Limiting Clinical Trial

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0039593
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0008976
enrolled or intend to participate in another clinical trial during the course of this study
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
a life expectancy of less than 2 years
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
history of continuous atrial fibrillation for the 6 months prior to screen visit
Beschrijving

Atrial Fibrillation disease length

Datatype

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0872146
two or more cardioversions, chemical or electrical, within the past 6 months prior to screen
Beschrijving

Chemical cardioversion Quantity | Electric Countershock Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C2585199
UMLS CUI [1,2]
C1265611
UMLS CUI [2,1]
C0013778
UMLS CUI [2,2]
C1265611
history of persistent second or third degree atrioventricular block
Beschrijving

Second degree atrioventricular block persistent | Complete atrioventricular block persistent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0264906
UMLS CUI [1,2]
C0205322
UMLS CUI [2,1]
C0151517
UMLS CUI [2,2]
C0205322
a prior implant of pacemaker or defibrillator device
Beschrijving

Implantation of cardiac pacemaker | Implantation of cardiac defibrillator

Datatype

boolean

Alias
UMLS CUI [1]
C0189842
UMLS CUI [2]
C0397417
a baseline, pre-paced qrs >120 ms on surface ecg
Beschrijving

Electrocardiogram QRS complex

Datatype

boolean

Alias
UMLS CUI [1]
C0429098
failure of the 1 to 1 atrioventricular conduction test
Beschrijving

1:1 atrioventricular conduction Test failed

Datatype

boolean

Alias
UMLS CUI [1,1]
C2215915
UMLS CUI [1,2]
C0039593
UMLS CUI [1,3]
C0231175
anticipated major cardiac surgery within the course of the study
Beschrijving

Cardiac Surgery Major Anticipated

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C0205164
UMLS CUI [1,3]
C3840775
Terug naar het begin van de pagina

Similar models

Eligibility Sick Sinus Syndrome NCT00284830

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
18 years of age and older
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
willing and able to give informed consent
boolean
C0021430 (UMLS CUI [1])
Clinical Study Follow-up Compliance behavior
Item
willing and able to comply with the study follow-up schedule
boolean
C3274571 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
Indication Dual Chamber Pacemaker Class
Item
class i/classii indications for dual chamber pacing
boolean
C3146298 (UMLS CUI [1,1])
C2911683 (UMLS CUI [1,2])
C3272276 (UMLS CUI [1,3])
DUAL CHAMBER IMPLANTABLE PULSE-GENERATOR Implantation Initial
Item
initial implant of a kappa 700, kappa 900, enpulse, or enrhythm dual chamber ipg
boolean
C0493526 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
C0205265 (UMLS CUI [1,3])
1:1 atrioventricular conduction | QRS interval | Intra-atrial pacing
Item
demonstrate 1 to 1 conduction and a qrs interval of < 120ms at 100 beats per minutes for a period of nine seconds while atrial pacing
boolean
C2215915 (UMLS CUI [1])
C2168881 (UMLS CUI [2])
C0199647 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Age
Item
less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
Informed Consent Unable | Informed Consent Unwilling
Item
unwilling or unable to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Clinical Study Follow-up Compliance behavior Lacking
Item
unwilling or unable to commit to follow-up schedule
boolean
C3274571 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Medical condition Excludes Testing | Medical condition Limiting Clinical Trial
Item
medical conditions that would preclude the testing required by the protocol or limit study participation
boolean
C3843040 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0039593 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
Study Subject Participation Status
Item
enrolled or intend to participate in another clinical trial during the course of this study
boolean
C2348568 (UMLS CUI [1])
Life Expectancy
Item
a life expectancy of less than 2 years
boolean
C0023671 (UMLS CUI [1])
Atrial Fibrillation disease length
Item
history of continuous atrial fibrillation for the 6 months prior to screen visit
boolean
C0004238 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Chemical cardioversion Quantity | Electric Countershock Quantity
Item
two or more cardioversions, chemical or electrical, within the past 6 months prior to screen
boolean
C2585199 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0013778 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
Second degree atrioventricular block persistent | Complete atrioventricular block persistent
Item
history of persistent second or third degree atrioventricular block
boolean
C0264906 (UMLS CUI [1,1])
C0205322 (UMLS CUI [1,2])
C0151517 (UMLS CUI [2,1])
C0205322 (UMLS CUI [2,2])
Implantation of cardiac pacemaker | Implantation of cardiac defibrillator
Item
a prior implant of pacemaker or defibrillator device
boolean
C0189842 (UMLS CUI [1])
C0397417 (UMLS CUI [2])
Electrocardiogram QRS complex
Item
a baseline, pre-paced qrs >120 ms on surface ecg
boolean
C0429098 (UMLS CUI [1])
1:1 atrioventricular conduction Test failed
Item
failure of the 1 to 1 atrioventricular conduction test
boolean
C2215915 (UMLS CUI [1,1])
C0039593 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
Cardiac Surgery Major Anticipated
Item
anticipated major cardiac surgery within the course of the study
boolean
C0018821 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C3840775 (UMLS CUI [1,3])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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