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

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

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00024996

Enrollment

120

Registered

2021-04-26

Start date

2021-05-14

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

R52.0

Interventions

Group 1: Standard therapy, Hospital specific concentration of local anesthetic Group 2: Use of Stimulation catheter and reduced concentration of local anesthetic, sham stimulation Group 3: Use of Stim

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

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

Secondary

Measure	Time frame
Degree of differential block, including Rivermead Assessment of Somatosensory Performance (RASP).	—

Countries

Germany

Contacts

Public ContactPatrick Moldzio

Universitätsklinikum Essen, Klinik für Anästhesiologie und Intensivmedizin, Direktor Prof. Dr. med. Th. Brenner

patrick.moldzio@uk-essen.de+4920172384749

Outcome results

None listed

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