Evaluation of Clinical and Biomechanical Correlation During Return to Sport After Anterior Cruciate Ligament Injury

Status

Terminated

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02686723

Acronym

REPILOG

Enrollment

Registered

2016-02-19

Start date

2016-02-29

Completion date

2016-12-31

Last updated

2020-03-17

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

Conditions

ACL Injury

Keywords

ACL injury, Return to sport, Motion analysis, Isokinetic evaluation, Risk factor

Brief summary

Comparison of two groups of subjets (ACL injury who return to sport) and control group non-injured about clinical and biomechanical data : * clinical test * functional test * motion analysis of 2 sport exercises * tibial translation * isokinetic evaluation

Detailed description

ACL injury in sport practice is frequent and after surgery subjects want to return to sport. Re injury during return to sport is significant and clinical and biomechanical risk factors are described. But no study investigate link between clinical and biomechanical during this risk period. The study will search to highlight correlation between clinical and biomechanical factors. Investigators will realize clinical evaluation (pain, translation) and functional tests (single hop test, triple hop test, 6m time hop test, crossover test). For biomechanical data, investigators will test 2 exercises in motion analyse laboratory (drop vertical jump and cutting task), a translation knee test with GnRB and isokinetic evaluation. Investigators will compared results of injured subjects with a control group non-injured.

Interventions

OTHERClinical and biomechanical evaluations

Clinical evaluation : demographics, clinic and functional testing. Biomechanical evaluation : isokinetic, motion analysis of 2 specific motion (drop vertical jump and cutting task) and anterior tibial translation with GnRB

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* surgeon repair ACL injury ; sport practice ; signed informed consent

Exclusion criteria

* for injury subjects: pain during cutting tasks ; associated injury with ACL rupture * for healthy subjects: history of ACL injury

Design outcomes

Primary

Measure	Time frame
Limb Symmetry Index	Day 0

Countries

France

Outcome results

None listed

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