ID

34134

Descrizione

Medtronic Reveal XT Study; ODM derived from: https://clinicaltrials.gov/show/NCT01526343

collegamento

https://clinicaltrials.gov/show/NCT01526343

Keywords

  1. 14/01/19 14/01/19 -
Titolare del copyright

see on clinicaltrials.gov

Caricato su

14 gennaio 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT01526343

Eligibility Atrial Fibrillation NCT01526343

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. patients undergoing planned, elective af surgery, either as a stand-alone procedure or as a concomitant cardiac operation.
Descrizione

ID.1

Tipo di dati

boolean

2. patients will have either a cox-maze procedure (full-biatrial lesion set) or surgical pulmonary vein isolation (pvi).
Descrizione

ID.2

Tipo di dati

boolean

3. patients 18 years or older.
Descrizione

ID.3

Tipo di dati

boolean

4. all eligible patients will be considered, regardless of gender or race.
Descrizione

ID.4

Tipo di dati

boolean

5. patients able and willing to provide informed consent and willing to comply with the required interval follow-up.
Descrizione

ID.5

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. patients with a preoperative permanent pacemaker.
Descrizione

ID.6

Tipo di dati

boolean

2. patients with a projected lifespan of less than six months.
Descrizione

ID.7

Tipo di dati

boolean

3. patients requiring emergent cardiac surgery.
Descrizione

ID.8

Tipo di dati

boolean

4. patients unwilling or unable to give written informed consent.
Descrizione

ID.9

Tipo di dati

boolean

5. patients undergoing a right atrial or left atrial lesion set procedure.
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Atrial Fibrillation NCT01526343

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
1. patients undergoing planned, elective af surgery, either as a stand-alone procedure or as a concomitant cardiac operation.
boolean
ID.2
Item
2. patients will have either a cox-maze procedure (full-biatrial lesion set) or surgical pulmonary vein isolation (pvi).
boolean
ID.3
Item
3. patients 18 years or older.
boolean
ID.4
Item
4. all eligible patients will be considered, regardless of gender or race.
boolean
ID.5
Item
5. patients able and willing to provide informed consent and willing to comply with the required interval follow-up.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
1. patients with a preoperative permanent pacemaker.
boolean
ID.7
Item
2. patients with a projected lifespan of less than six months.
boolean
ID.8
Item
3. patients requiring emergent cardiac surgery.
boolean
ID.9
Item
4. patients unwilling or unable to give written informed consent.
boolean
ID.10
Item
5. patients undergoing a right atrial or left atrial lesion set procedure.
boolean

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