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Prospective evaluation of complications after percutaneous cannulation of the internal jugular vein for minimal invasive cardiac surgery

Prospective evaluation of complications after percutaneous cannulation of the internal jugular vein for minimal invasive cardiac surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00035663
Enrollment
102
Registered
2024-12-09
Start date
2024-12-09
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I80

Interventions

Group 1: Patients over the age of 18 who are undergoing minimally invasive cardiac surgery using a Cardiopulmonary bypass (CPB), in which the internal jugular vein is cannulated for this purpose. A c

Sponsors

Universitätsklinikum Bonn, Klinik für Anästhesiologie und Operative Intensivmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Minimally invasive cardiac surgery using a heart-lung machine, with and without venous cannulation of the internal jugular vein

Exclusion criteria

Exclusion criteria: - Age <18 years - Pre-existing occlusion of the internal jugular vein - Pre-existing thrombosis of the internal jugular vein - Known prothrombotic coagulopathy - Catheterisation of the VJI within 14 days before surgery - Pre-existing anatomical anomaly of the internal jugular vein

Design outcomes

Primary

MeasureTime frame
Comparison of the incidence of sonographically detectable thrombi in the internal jugular vein (IJV) between patients with and without venous cannulation following minimally invasive cardiac surgery using a heart-lung machine.

Secondary

MeasureTime frame
- Puncture technique and number of possible incorrect punctures of the internal jugular vein - Development of a haematoma after puncture - If a thrombus is detectable: size of the thrombus - Obstruction of the venous outflow due to an thrombus - Pre-existing anticoagulant treatment of the patient - Complaints due to the detection of a thrombus - Complications due to the thrombus - Comparison between the observation groups

Countries

Germany

Contacts

Public ContactFlorian Piekarski

Universitätsklinikum Bonn, Klinik für Anästhesiologie und Operative Intensivmedizin

florian.piekarski@ukbonn.de+49 228-287-0

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026