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The Influence of Wedge Insoles After Partial Meniscectomy

Effect of Orthotic Devices in the Recovery After Partial Meniscectomy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02190188
Enrollment
63
Registered
2014-07-15
Start date
2014-03-31
Completion date
2018-01-01
Last updated
2018-03-23

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

Conditions

Partial Meniscectomy

Keywords

wedge insoles,, knee brace,, orthotic device, goal

Brief summary

Research on the implications of orthotic devices and the recovery after knee arthroscopy are widely known. But only a handful of specific issues have been studied to date. However, the effect of orthotic devices on the recovery after partial meniscectomy are largely unknown. To our best knowledge, there are no studies that deal with the treatment of partial medial or lateral meniscectomy with wedge insoles, valgus or varus knee braces. The purpose of this study is to find out if using wedge inserts or knee orthoses improve the outcomes after partial meniscectomy. We therefore verify the following hypothesis: In patients with partial meniscectomy can be by the postoperative use of exculpatory wedge deposits or relieving knee brace achieve a significantly better clinical outcome than without specific treatment.

Interventions

DEVICEWedge Insole 5mm

Sponsors

Medical University Innsbruck
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* full leg x-ray to measure the leg axis * undersigned Informed Consent Form

Exclusion criteria

* at the same time conducted or within one year subsequent corrective osteotomies of the leg axis * medial meniscectomy combination and valgus * combination of lateral meniscectomy and varus * psychiatric or neurological comorbidities that produce a poor compliance * forth degree cartilage lesions or evident osteoarthritis * concomitant lesion of the collateral ligaments * insufficient knowledge of the study language

Design outcomes

Primary

MeasureTime frame
Knee-specific questionnaires which combine an activity and a quality of life score.Two years

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026