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Comparison of the influence of saphenous and femoralis blockade on postoperative pain intensity and on muscle strength in patients after surgical procedures on the lower extremities

Comparison of the influence of saphenous and femoralis blockade on postoperative pain intensity and on muscle strength in patients after surgical procedures on the lower extremities - SAFE-Knie

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00030078
Enrollment
13495
Registered
2022-08-25
Start date
2021-09-10
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

surgery of lower extremity

Interventions

Group 1: Patients with saphenous blockage after orthopaedic surgery are evaluated regarding muscle strength (JANDA) Group 2: Patients with saphenous blockage after orthopaedic surgery are evaluated r

Sponsors

Charité Universitätsmedizin Berlin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Adult patients - Saphenous blockade by single shot or catheter procedure - Femoral blockade by single shot or catheter procedure - Ischial blockade by catheter procedure in combination with saphenous or femoral blockade - Documented postoperative visits (at least one visit) to monitor pain intensity and assess mobility.

Exclusion criteria

Exclusion criteria: - ambiguous assignment of a regional procedure - postoperative visits not documented or not fully documented

Design outcomes

Primary

MeasureTime frame
- Motor strenghth impairment (degree of strength according to Janda, quadriceps femoris muscle)

Secondary

MeasureTime frame
- postoperative pain intensity (NRS at rest and movement) - Pain medication consumption during inpatient stay

Countries

Germany

Contacts

Public ContactSascha Tafelski

Charité Universitätsmedizin Berlin

sascha.tafelski@charite.de030 450531014

Outcome results

None listed

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