Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT05598385

Groin Complications in Open Vs. Percutaneous Peripheral Cannulation in Minimally Invasive Cardiac Surgery

Groin Complications in Open Vs. Percutaneous Peripheral Cannulation for Cardiopulmonary Bypass in Minimally Invasive Cardiac Surgery

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Jessa Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this randomized trial is to investigate the groin complications in open vs percutaneous peripheral cannulation for cardiopulmonary bypass in minimally invasive cardiac surgery

Detailed description

The femoral artery (FA) and vein (FV) are considered the preferred site for peripheral cannulation during cardiac surgery. Normally, a small incision is made to access the FA and FV, which is also called open surgical cannulation. Afterwards, the incision site is traditionally closed with sutures (1, 2). However, groin complications such as hematoma, access-site infection and fistulas are complications that can eventually lead to a longer hospital stay (3). Recently, suture-mediated closure systems (SMCS) have been developed to achieve hemostasis (4). This allows for percutaneous cannulation. Still, little is known about the effects on groin complications after percutaneous cannulation in cardiac surgery. Therefore, a prospective randomized study is now being conducted to investigate the groin complications in open vs. percutaneous peripheral cannulation for cardiopulmonary bypass in minimally invasive cardiac surgery.

Conditions

Interventions

TypeNameDescription
PROCEDUREOpen cannulationA small incision is made to access the FA and FA. Afterwards, the incision site is traditionally closed with sutures.
PROCEDUREPercutaneous cannulationCannulation is performed through a suture-mediated closure system.

Timeline

Start date
2024-11-01
Primary completion
2024-11-09
Completion
2024-11-09
First posted
2022-10-28
Last updated
2024-11-29

Source: ClinicalTrials.gov record NCT05598385. Inclusion in this directory is not an endorsement.