Informatie:
Fout:
ID
34134
Beschrijving
Medtronic Reveal XT Study; ODM derived from: https://clinicaltrials.gov/show/NCT01526343
Link
https://clinicaltrials.gov/show/NCT01526343
Trefwoorden
Versies (1)
- 14-01-19 14-01-19 -
Houder van rechten
see on clinicaltrials.gov
Geüploaded op
14 januari 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01526343
Eligibility Atrial Fibrillation NCT01526343
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01526343
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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
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