Ultrasound Guidance for Axillary Plexus Regional Anesthesia

Ultrasound Guidance for Axillary Plexus Regional Anesthesia - AxPlex

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00006037

Enrollment

100

Registered

2014-03-29

Start date

2014-04-14

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

axillary plexus regional anesthesia

Interventions

Group 1: axillary plexus block - navigation assisted ultrasound Group 2: axillary plexus block - conventional ultrasound

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with planned Hand-forarm surgery Age>18 years ASA classification I, II and III Bodyweight 50-120kg Written informed consent for study participation / informed consent for regional anesthesia

Exclusion criteria

Exclusion criteria: Age < 18 Years No Informed Consent for study participation / regional anesthesia inflammation in the planned puncture site for regional anesthesia pregnancy Patients that, due to prior medical conditions, did not receive anesthesiologic clearance for surgical therapy

Design outcomes

Primary

Measure	Time frame
Percieved pain measured on a numeric rating scale from 0(no pain) to 100(maximum pain), recorded directly after completion of axillary plexus block	—

Secondary

Measure	Time frame
Time intervall between axillary block application and establishment of adequate anesthesia allowing surgical therapy	—

Countries

Germany

Contacts

Public ContactVolker Schick

Uniklinik KölnKlinik für Anästhesiologie und Operative Intensivmedizin

volker.schick@uk-koeln.de02214786283

Outcome results

None listed

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