Proof of concept and Pilot Study for combined electro-chemical Nerveblock in a perioperative setting

Not Applicable

Recruiting

• Conditions: R52.0; Acute pain

• Registration Number: DRKS00024996
• Lead Sponsor: niversitätsklinikum Essen, Klinik für Anästhesiologie und Intensivmedizin, Direktor Prof. Dr. med. Th. Brenner

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-04-26
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

in-patients with surgery of the upper or lower extremity and regional anesthesia, written consent

Exclusion Criteria

chronic pain patients, any type of neuropathy, Treatment with pacemaker device

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Amount of local anesthetics, amount of used opiods during the perioperative period, Pain Score (VAS/NRS)

Secondary Outcome Measures

Name	Time	Method
Degree of differential block, including Rivermead Assessment of Somatosensory Performance (RASP).