Trials / Terminated
TerminatedNCT03001141
Study Protocol/ Registry of MultiPoint™ Pacing in Brazil
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 200 (actual)
- Sponsor
- Abbott Medical Devices · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective, multicenter, non-randomized registry/observational study. The study will enroll up to 200 patients with successful St. Jude Medical (SJM) Cardiac Resynchronization Therapy (CRT) MP device implant from up to 10 centers.
Detailed description
Any patient receiving a market-approved SJM Quadra Assura MP (CRT-D) or newer model quadripolar device with MPP capability and who meets the inclusion criteria and none of the exclusion criteria is eligible for enrollment in the study. Patients will be followed for 12 months after implant. Data will be collected after device implant (up to 30 days after successful implant), at 3, 6 and 12 months post-implant and during unscheduled visits.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Observational | Device: MultiPoint Pacing will be enabled in enrolled patients at the discretion of the physician. |
Timeline
- Start date
- 2017-05-18
- Primary completion
- 2018-04-18
- Completion
- 2019-02-08
- First posted
- 2016-12-22
- Last updated
- 2019-09-16
Locations
4 sites across 1 country: Brazil
Source: ClinicalTrials.gov record NCT03001141. Inclusion in this directory is not an endorsement.