Information:
Fel:
ID
34134
Beskrivning
Medtronic Reveal XT Study; ODM derived from: https://clinicaltrials.gov/show/NCT01526343
Länk
https://clinicaltrials.gov/show/NCT01526343
Nyckelord
Versioner (1)
- 2019-01-14 2019-01-14 -
Rättsinnehavare
see on clinicaltrials.gov
Uppladdad den
14 januari 2019
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Atrial Fibrillation NCT01526343
Eligibility Atrial Fibrillation NCT01526343
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01526343
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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