Trials / Terminated
TerminatedNCT02858245
A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgitation Subjects Receiving the MitraClip® Device
A Feasibility Registry on Use of Actigraphy Monitoring in Degenerative Mitral Regurgitation (DMR) Subjects Receiving the MitraClip® Device
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 30 (actual)
- Sponsor
- Abbott Medical Devices · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A prospective, open-label, and multi-centered feasibility registry.
Detailed description
This is a prospective, open-label, and multi-centered feasibility registry (single arm study). Approximately 36 subjects with prohibitive risk degenerative mitral regurgitation (DMR) who receive at least 1 commercial MitraClip will be registered at up to 10 US sites.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | No intervention - registry |
Timeline
- Start date
- 2016-11-01
- Primary completion
- 2017-12-01
- Completion
- 2017-12-01
- First posted
- 2016-08-08
- Last updated
- 2018-05-07
Locations
8 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT02858245. Inclusion in this directory is not an endorsement.