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In-plane cannulation of the brachiocephalic with needle-guide

In-plane cannulation of the brachiocephalic with needle-guide - /

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00012343
Enrollment
132
Registered
2017-07-04
Start date
2013-11-17
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

In-house patients, who require the placement of a central venous catheter (CVC) for their therapy / treatment.

Interventions

Group 1: Ultrasound-guided cannulation of the brachiocephalic by freehand-technique. Group 2: Ultrasound-guided cannulation of the brachiocephalic with the use of a needle-guide.

Sponsors

BG Universitätsklinikum BergmannsheilKlinik für Anästhesiologie, Intensiv-, Palliativ- und Schmerzmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - The need to place a CVC for the operation / treatment - Informed written consent

Exclusion criteria

Exclusion criteria: - Disability to understand the investigation - No need for central venous catheter placement - Denial of study participation - Conditions that hinder a CVC placement into into the brachiocphalic vein

Design outcomes

Primary

MeasureTime frame
Time to successful cannulation of the brachiocephalic vein. Measured in seconds from skin-entry to visual depiction of the needle inside the brachiocephalic vein and aspiration of blood. Analysis is performed post procedural with the aid of video- and ultrasound recordings.

Secondary

MeasureTime frame
Visibility of the needle during the procedure. Measured in seconds and depicted as percentage of the primary study criterion. Analysis is performed post procedural with the aid of video- and ultrasound recordings.

Countries

Germany

Contacts

Public ContactTim Mäcken

BG Universitätsklinikum BergmannsheilKlinik für Anästhesiologie, Intensiv-, Palliativ- und Schmerzmedizin

tim.maecken@rub.de02343023666

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026