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Venous Access clinical trials

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NCT ID: NCT05519787 Completed - Chemotherapy Clinical Trials

A Retrospective, Observational, Monocenter, Study to Describe the Utilization and Overall Safety and Performance of POLYSITE®/SEESITE® Implantable Ports

Start date: December 14, 2021
Phase:
Study type: Observational

This study is a retrospective, observational, monocenter case series. The purpose of this study is to collect clinical data to describe the use of POLYSITE® and SEESITE® devices and verify overall safety and performance. This study is part of the Post-Market Clinical Follow-up (PMCF) activities of the PEROUSE MEDICAL manufacturer. The primary data source for this study was patient's medical records from a French Hospital. The study population was defined as all patients who did receive POLYSITE® and SEESITE®. Data from a minimum of 50 patients were planned for the statistical review.

NCT ID: NCT04382430 Completed - Clinical trials for Ultrasound Therapy; Complications

Ultrasound Axillary Vein Access: Evaluation of Learning Curve for an Alternative Approach to Cardiac Device Implantation

Start date: May 28, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the learning curve associated with Ultrasound (US) guided axillary vein access for cardiac device implantation based on length of procedure among operators of various levels of experience and to assess the 30-day complication rate for patients undergoing US guided device placement versus traditional implant methods.

NCT ID: NCT04234347 Not yet recruiting - Venous Access Clinical Trials

Long Versus Short Axis Approach for Ultrasound Guided Peripheral Intravenous Access

Start date: May 1, 2024
Phase: N/A
Study type: Interventional

To compare a long axis approach versus short axis when placing peripheral IVs using ultrasound guidance.

NCT ID: NCT04036734 Completed - Varicose Veins Clinical Trials

Longitudinal or Transverse Orientation of Ultrasound Probe in Minimally Invasive Venous Surgery.

Start date: July 24, 2019
Phase: N/A
Study type: Interventional

Longitudinal ultrasound orientation during central venous cannulation has been suggested by a number of radomised studies to offer superior cannulation rates. This technique may offer a simple, safe and cost-neutral step to improve cannulation rates in the widely performed minimally invasive endovenous intervention.