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Long term Follow-Up after ACL reconstruction

Long term Follow-Up after ACL reconstruction - ACL Follow-Up Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42229
Enrollment
100
Registered
2015-09-30
Start date
2016-08-29
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

ACL tear anterior cruciate ligament rupture

Interventions

Sponsors

Medisch Centrum Alkmaar
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria:;• Unilateral ACL rupture; • Suitable to one of the subgroups; • Can be contacted; • Are willing and able to participate in the study protocol and follow-up visitation of the outpatient clinic

Exclusion criteria

Exclusion criteria: Subjects will be excluded when they:;• are not willing to participate; • are not capable of participating (either mentally or physically); • have deceased; • are unable to undergo radiography (e.g. due to pregnancy).

Design outcomes

Primary

MeasureTime frame
Radiographic outcome measures • Evidence of osteoarthritis based on Kellgren-Lawrence scale Clinical outcome measures • Range of Motion • Knee stability

Secondary

MeasureTime frame
• Quality of Life • Pain • Status of return to work and daily activities • Secondary surgical procedures • Surgical complication • Patient characteristics

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)