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Quality assurance in postoperative pain management comparing adductor canal block at the apex (ACB) and a higher-volume and low-concentration femoral nerve block (NFB) in the groin with positioning in patients undergoing total knee arthroplasty (TKA) under general anesthesia

Quality assurance in postoperative pain management comparing adductor canal block at the apex (ACB) and a higher-volume and low-concentration femoral nerve block (NFB) in the groin with positioning in patients undergoing total knee arthroplasty (TKA) under general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036838
Enrollment
240
Registered
2025-06-16
Start date
2025-07-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

M17

Interventions

Group 1: Application of a femoral nerve block in the groin (NFB) with Naropin 0.25% 40 ml Group 2: Application of a femoral nerve block in the groin (NFB) with Naropin 0.25% 40 ml and head-down positi

Sponsors

Katholisches Klinikum Bochum, Martin-Luther Krankenhaus
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • All patients undergoing primary bicondylar total knee arthroplasty (TKA) at the Martin Luther Hospital Bochum-Wattenscheid, part of the Catholic Hospital Bochum, between 2025 and 2026. • Anesthesia: General anesthesia • Age 18 or older • ASA I-III • Patient consent

Exclusion criteria

Exclusion criteria: • Younger than 18 years • Anesthesia procedure: Spinal anesthesia • Pregnancy • Joint infection, such as periprosthetic joint infection (PJI) and history of PJI • ASA IV • Allergies to local anesthetics • Infection of the puncture site • Failure to sign a consent form and patient refusal • Dementia or inability to cooperate • Language barrier • Alcohol dependence

Design outcomes

Primary

MeasureTime frame
• Cumulative amount of additional opioid analgesics administered up to the first postoperative day

Secondary

MeasureTime frame
• Time to first opioid in minutes • Pain intensity: Change in NRS pain score on the day of surgery (0-10) • Pain intensity: Change in NRS pain score on the first postoperative day (0-10) • Degree of quadriceps weakness after the block on the blocked and operated side, muscle strength assessment (Manual Muscle Test = MMT) • Time the patient first got out of bed • Duration of first getting out of bed • Time the patient first walked with a walking aid under the guidance of a rehabilitation physician and physiotherapist

Countries

Germany

Contacts

Public ContactAlexander Andres, MHBA

Katholisches Klinikum Bochum, Martin-Luther Krankenhaus

alexander.andres@klinikum-bochum.de+492327657300

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026