Eligibility Atrial Fibrillation NCT01526343

Inclusion Criteria
Beschreibung

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.
Beschreibung

ID.1

Datentyp

boolean

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

ID.2

Datentyp

boolean

3. patients 18 years or older.
Beschreibung

ID.3

Datentyp

boolean

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

ID.4

Datentyp

boolean

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

ID.5

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

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

ID.6

Datentyp

boolean

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

ID.7

Datentyp

boolean

3. patients requiring emergent cardiac surgery.
Beschreibung

ID.8

Datentyp

boolean

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

ID.9

Datentyp

boolean

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

ID.10

Datentyp

boolean

Ähnliche Modelle

Eligibility Atrial Fibrillation NCT01526343

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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