Clinical and biomechanical Analysis of preoperative brace-testing in medial-open high tibial osteotomy

Clinical and biomechanical Analysis of preoperative brace-testing in medial-open high tibial osteotomy - HTO-Str-UKL

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00025303

Enrollment

Registered

2021-06-10

Start date

2021-05-25

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 M21.16

Interventions

Group 1: Patients suffering from medial gonarthritis with varus malalignement will undergo biomechanical and neuromechanical analysis in a 3d motion laboratory following orthosis-basid correction of t

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Medial varusgonarthritis with a principal indication for high tibial osteotomy

Exclusion criteria

Exclusion criteria: previous surgery affectingb the mechanical alignement of the leg, history of neurological impairments that affect the general neuromuscular activation during gait

Design outcomes

Primary

Measure	Time frame
varus/valgus alignement of the leg which is measured at timepoints 0, then 3 and 6 weeks after the start of wearing the brace and another follow up at 3 months following the osteotomy.	—

Secondary

Measure	Time frame
patient reported outcome and neuromuscular activation pattern at the same timepoints as the primary outcome, additionally the PRO-measures will be collected again at 12 months postoperatively.	—

Countries

Germany

Contacts

Public ContactGerrit Bode

Sporthopaedicum Straubing

bode@sporthopaedicum.de+49 9421 99570

Outcome results

None listed

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