Trials / Terminated
TerminatedNCT04552665
Prospective Procedural Data Collection for Continuous Improvement of the KODEX - EPD™ System Performance.
Prospective Procedural Data Collection for Continuous Improvement of the KODEX - EPD™ System Performance
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 30 (actual)
- Sponsor
- EPD Solutions, A Philips Company · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the KODEX EPD Field study is to evaluate the performance of the KODEX-EPD system and collect procedural data and medical images for Philips' internal research and development activities (R\&D) related to the KODEX-EPD system, as well as for marketing and publication purposes. The KODEX-EPD system is an imaging system that will allow for real time visualization of the catheters in your heart during your procedure, as well as display cardiac images of your heart in several different formats.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | KODEX-EPD system | To evaluate the performance of the KODEX-EPD system and collect procedural data and medical images for Philips' internal research and development activities (R\&D) |
Timeline
- Start date
- 2020-10-28
- Primary completion
- 2023-06-06
- Completion
- 2023-06-06
- First posted
- 2020-09-17
- Last updated
- 2023-06-08
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04552665. Inclusion in this directory is not an endorsement.