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Prospective Observational Study of the Power PICC Family of Devices and Accessories

NCT04263649 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 450

Last updated 2024-08-19

Study results available
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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.

Conditions

  • Peripherally Inserted Central Catheter

Interventions

DEVICE

Peripherally Inserted Central Catheter

insertion of a Peripherally Inserted Central Catheter (PICC)

Sponsors & Collaborators

  • FGK Clinical Research GmbH

    collaborator INDUSTRY

  • Becton, Dickinson and Company

    lead INDUSTRY

Principal Investigators

  • Klaus Hoerauf, MD · Becton, Dickinson and Company

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-18
Primary Completion
2022-01-05
Completion
2022-01-05
FDA Device
Yes

Countries

  • Austria
  • Belgium
  • Czechia
  • Denmark
  • Germany
  • Italy
  • Netherlands
  • Spain
  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04263649 on ClinicalTrials.gov