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Functional Performance after Ligamys surgery, a case matched study.

Functional Performance after Ligamys surgery, a case matched study. - Ligamys propriocepsis trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48879
Enrollment
96
Registered
2018-07-23
Start date
2018-09-17
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

ACL healing ACL reconstruction

Interventions

None listed

Sponsors

Stichting SCORE
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Male or Female Sporters aged 21-45 Ligamys operation 12-36 months postoperative ;Control group match on age/ sex/ sports

Exclusion criteria

Exclusion criteria: History of fracture in lower extremity Recent hip/ knee/ ankle pathologies less dan 2 year ago, other than ligamys Intra articulair damage lower extremity

Design outcomes

Primary

MeasureTime frame
The primary purpose of this study is to report the functional performance after Ligamys surgery. The expactation is that the Ligamys method will achieve the 90% LSI (Limb Symmetry Index is used to identify functional assymetry, and is measured as follow: test score affected leg / testscore non affected leg x 100%.) benchmark at the hoptests and less than 9% difference with the matched control group.

Secondary

MeasureTime frame
As a secondary outcome, the other hop tests and joint position sense tests will be measured. Also the IKDC and Tegner questionnaire will be used.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)