Analgesic consumption and mobilization ability under concomitant regional anesthesia in patients undergoing total knee arthroplasty

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00033517

Enrollment

300

Registered

2024-01-31

Start date

2024-01-26

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

M17

Interventions

Group 1: Blockade of the femoral nerve/sciatic nerve: Retrospective assessment of perioperative opioid requirements, pain level, necessary co-analgesics and length of hospital stay under concomitant r

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: primaräy total knee arthroplasty under concomitant peripheral regional anesthesia in the years 2021 to 2025

Exclusion criteria

Exclusion criteria: Non-Compliance to the including criteria’s

Design outcomes

Primary

Measure	Time frame
Retrospective study of the course of patients after total knee atrhoplasty under concomitant peripheral regional anesthesia. The focus is on assessing the accompanying intraoperative intravenous opioid and anesthetic administration as a sign of failure of peripheral regional anesthesia, as well as the postoperative opioid requirement.	—

Secondary

Measure	Time frame
Recording the length of hospital stay and the mobilization distance.	—

Countries

Germany

Contacts

Public ContactSebastian d

Klinik für Anaesthesiologie Universitätsklinikum Heidelberg

sebastian.decker@med.uni-heidelberg.de+49 (0) 6221-56 61 10

Outcome results

None listed

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