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"Patientexpectation Following Osteotomy Around the Knee"

"Patientexpectation Following Osteotomy Around the Knee"

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00007613
Enrollment
150
Registered
2014-12-18
Start date
2015-01-15
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

M17

Interventions

Group 1: In patients with indication for osteotomy around the knee (high tibial osteotomy: HTO, distal femur osteotomy: DFO) patient expecation and fulfillment (12-18m after surgery) is evaluated by u

Sponsors

Deutsche Kniegesellschaft e.V.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: focal chondral lesion (ICRS 3/4), varusgonarthrosis (Kellgren Lawrence 3/4) with varus/valgus alignment >2°, indication for osteotomy around the knee, written consent

Exclusion criteria

Exclusion criteria: denial to participate, rheumatism, diabetes, chronic pain syndrom, alcohol-/drugabuse, kneeinstability, concomitant chondral therapy, denial to participate

Design outcomes

Primary

MeasureTime frame
Standardized preoperative patient expectation on osteotomies around the knee, using the score by Mancuso et al.

Secondary

MeasureTime frame
1) Knee and Osteoarthritis Outcome Score (KOOS): preop. and 12-18 months after surgery. 2) General Self-Efficacy Scale -GSE- by Jerusalem and Schwarzer: Preop 3) Standardised Fulfillment by Andrews and Withey: 12-18 months postop.

Countries

Germany

Contacts

Public ContactTim Saier

BGU Murnau

tim.saier@bgu-murnau.de+49 (0)8841 48 4802

Outcome results

None listed

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