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Dislocation rates of perineural catheters: a volunteer study

Dislocation rates of perineural catheters: a volunteer study - Catheterdislocation study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00003494
Enrollment
20
Registered
2012-11-13
Start date
2012-11-04
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

Healthy participants

Interventions

Group 1: 20 male, healthy volunteers get a femoral nerve catheter and a scalaenus catheter and have to practice standardized movements intermittently.

Sponsors

Universitätsklinik für Klinische Pharmakologie
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: •Healthy males aged between 18 and 45 years •BMI < 30 kg/m2 •Written informed consent given by volunteers after being provided with detailed information about the nature, risks, and scope of the clinical study as well as the expected desirable and adverse effects of the drug •No legal incapacity and/or other circumstances rendering the subject unable to understand the nature, scope and possible consequences of the study

Exclusion criteria

Exclusion criteria: •Anatomical abnormalities of the upper or lower limbs •BMI >30 kg/m2 •Use of NSAID during the last 2 weeks •Known allergy or hypersensitivity against mepivacaine or amino-amide local anaesthetics •Participation in another clinical study within the last 4 weeks prior to study •Coagulopathy •Abnormalities in ECG that are considered clinically relevant like AV-block or bradykardia •Unreliability and/or lack of cooperation •Inability to perform the standardized physical exercises (definition see below) •Other objections to participate in the study in the opinion of the investigator

Design outcomes

Primary

MeasureTime frame
Two different nerve catheters are located with the help of ultrasound. Each volunteer has to perform physiotherapeutic exercises hourly all together for 3 times. After these exercises the volunteer has to undergo an ultrasound examination to evaluate catheter postion. After 3 runs volunteers should do daily routine activities for 2hours. After this procedure a final ultrasound examination take place. The dislocation rate are evaluated.

Secondary

MeasureTime frame
no secondary outcome

Countries

Austria

Contacts

Public ContactDaniela Marhofer

Universitätsklinik für Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie

daniela.marhofer@meduniwien.ac.at+43 1 40400n 4107

Outcome results

None listed

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