Eligibility Atrial Fibrillation NCT01526343

Inclusion Criteria
Beschrijving

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.
Beschrijving

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

3. patients 18 years or older.
Beschrijving

ID.3

Datatype

boolean

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

ID.4

Datatype

boolean

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

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

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

ID.6

Datatype

boolean

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

ID.7

Datatype

boolean

3. patients requiring emergent cardiac surgery.
Beschrijving

ID.8

Datatype

boolean

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

ID.9

Datatype

boolean

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

ID.10

Datatype

boolean

Similar models

Eligibility Atrial Fibrillation NCT01526343

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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