Trials / Completed
CompletedNCT05209828
Post-market Clinical Follow-up of Pfmmedical Ports
Prospective, Monocentric Observational Study on the Clinical Use and Patient Satisfaction of Pfmmedical Implantable Vascular Access Ports
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 149 (actual)
- Sponsor
- pfm medical gmbh · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Prospective, monocentric, non-randomised, observational post-market clinical follow-up study in Germany to obtain post-market information on the pfmmedical ports with a follow-up (FU) of 6 months. The focus is on patient reported satisfaction, clinical application, and complication rates.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | pfmmedical implantable vascular access ports | Implantion of an implantable vascular access port which facilitates repeated vascular access intended for the delivery of medications, intravenous fluids, parenteral nutrition solutions or blood products and blood sampling using a Huber needle. |
Timeline
- Start date
- 2022-04-13
- Primary completion
- 2023-03-09
- Completion
- 2023-03-09
- First posted
- 2022-01-27
- Last updated
- 2024-04-05
Locations
1 site across 1 country: Germany
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05209828. Inclusion in this directory is not an endorsement.