Trials / Completed
CompletedNCT04263649
Prospective Observational Study of the Power PICC Family of Devices and Accessories
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 450 (actual)
- Sponsor
- Becton, Dickinson and Company · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Post-market, observational study to collect prospective data related to the safety and performance of the Power PICC family of devices and its accessories in a real-world setting.
Detailed description
Single-arm, post-market, observational, prospective study to asses the safety and performance of the Power PICC Power PICC family of devices and its accessories in a real-world setting. The study will only enroll patients that need a Power PICC catheter as part of their medical care. Patients will be followed from insertion through removal, or up to 180 days (whichever comes first). Data collected will be gathered from the patient's medical chart.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Peripherally Inserted Central Catheter | insertion of a Peripherally Inserted Central Catheter (PICC) |
Timeline
- Start date
- 2020-06-18
- Primary completion
- 2022-01-05
- Completion
- 2022-01-05
- First posted
- 2020-02-11
- Last updated
- 2024-08-19
- Results posted
- 2024-08-19
Locations
14 sites across 9 countries: Austria, Belgium, Czechia, Denmark, Germany, Italy, Netherlands, Spain, Switzerland
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04263649. Inclusion in this directory is not an endorsement.