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Clinical and Functional Outcomes 2 Years After ACL Repair and InternalBrace Ligament Augmentation in Comparison With ACL Reconstruction

NCT04429165 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 68

Last updated 2023-01-19

No results posted yet for this study

Summary

The aim of this study is to assess the clinical, biomechanical and functional outcome 2 years after anterior cruciate ligament (ACL) repair and InternalBraceTM augmentation now in direct comparison to ACL reconstruction and to identify potential deficits compared to the contralateral healthy side as well as with a knee-healthy age-matched collective. In addition, socio-economic aspects such as return to work and sports and treatment cost will be compared between both techniques.

Conditions

  • Injury of the Anterior Cruciate Ligament (ACL)

Interventions

OTHER

collection of Patient Reported Outcome (PRO) data

collection of Patient Reported Outcome (PRO) data by questionnaires

OTHER

collection of anthropometric and clinical functional data

collection of anthropometric and clinical functional data including range of motion (ROM), isokinetic muscle strength, joint position sense, single leg balance ability, and muscle activity

OTHER

gait analysis

gait analysis in a motion capture volume on a walkway including force plates and on a treadmill with pressure plates, while 3D kinematics and kinetics, pressure and electromyographic (EMG) data will be recorded

Sponsors & Collaborators

  • University Hospital, Basel, Switzerland

    lead OTHER

Principal Investigators

  • Sebastian Mueller, Dr. med. · Department of Orthopaedics and Traumatology, University Hospital Basel

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-04-23
Primary Completion
2022-07-14
Completion
2022-07-14

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04429165 on ClinicalTrials.gov