Trials / Unknown
UnknownNCT02506621
ELR Monitoring Against Permanent Pacemaker in Atrial Fibrillation
Randomised ELR Monitoring Against Permanent Pacemaker in Atrial Fibrillation
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- Sponsor
- Eastbourne General Hospital · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Randomised crossover study comparing the sensitivity and specificity of 5 External loop recorders in detecting pacemaker detected Atrial fibrillation burden.
Detailed description
The purpose of the study is to compare the diagnostic accuracy of the ZIO xt , MoMe, TECHNOMED pocket ECG and Nuubo to the R-test, our current standard clinical practice, in detection of AF burden, in patients with history of Paroxysmal Atrial Fibrillation and have a dual chamber pacemaker or ICD in situ, with sensitivity and specificity of AF detection calculated from the implanted pacemaker monitored beat to beat holters.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | R test | |
| DEVICE | Nuubo | |
| DEVICE | TECHNOMED pocket ECG | |
| DEVICE | ZIO xt patch | |
| DEVICE | MoMe |
Timeline
- Start date
- 2015-09-01
- Primary completion
- 2015-12-01
- Completion
- 2016-01-01
- First posted
- 2015-07-23
- Last updated
- 2015-07-23
Source: ClinicalTrials.gov record NCT02506621. Inclusion in this directory is not an endorsement.