Eligibility Atrial Fibrillation NCT01526343

Inclusion Criteria
Description

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.
Description

ID.1

Type de données

boolean

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

ID.2

Type de données

boolean

3. patients 18 years or older.
Description

ID.3

Type de données

boolean

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

ID.4

Type de données

boolean

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

ID.5

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.6

Type de données

boolean

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

ID.7

Type de données

boolean

3. patients requiring emergent cardiac surgery.
Description

ID.8

Type de données

boolean

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

ID.9

Type de données

boolean

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

ID.10

Type de données

boolean

Similar models

Eligibility Atrial Fibrillation NCT01526343

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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