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Hamstring Stiffness After Anterior Cruciate Ligament Reconstruction

Hamstring Stiffness After Anterior Cruciate Ligament Reconstruction: a Prospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05264597
Acronym
ACLSTIFF
Enrollment
135
Registered
2022-03-03
Start date
2017-01-01
Completion date
2021-10-01
Last updated
2025-03-26

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

Conditions

ACL Injury, Sport Injury, Stiffness of Knee, Not Elsewhere Classified

Brief summary

The role of hamstring has been studied in anterior cruciate ligament (ACL) injury prevention, mainly to counteract the anterior tibial translation , especially when contracting eccentrically, but also with passive stiffness. However, little is known about the passive hamstring stiffness after ACL reconstruction (ACLR). The primary objective of this study is to evaluate the passive stiffness of hamstring muscles after ACLR by using an isokinetic device. Secondary, we aimed to test the individual and surgical characteristics associated with hamstring stiffness and the impact of hamstring stiffness on RTS and knee re-injury. The hypotheses are that hamstring stiffness will be lower in the ACLR leg compared to the uninjured leg and to healthy individuals. Also, we hypothesized that hamstring stiffness will be lower after hamstring autograft compared to patellar tendon autograft and will increase progressively after ACLR to be symmetrical at the time for RTS. Also, we hypothesized that hamstring stiffness could be associated with better outcomes at RTS (RTS at same level and lower re-injury rates)

Interventions

None listed

Sponsors

University Hospital, Caen
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients who have had an ACL reconstruction surgery (isolated or associated with other meniscal or ligamentary surgery) * Patient included in the sport medicine follow-up protocole with intermediate and final isokinetic muscular assessment at 4 months and 8 mnths after surgery respectively * Patient who received the information form

Exclusion criteria

* Patient who did not participate in all follow-up consultations and isokinetic muscular assessments * Cognitive or sensory impairment making it impossible to understand the information form * Neurological, traumatic or osteoarticular history responsible for muscle imbalance prior to surgery * Previous severe injury on the ipsilateral or contralateral knee * Recent muscle damage * ACL reinjury ( graft failure) * Patient with genu flexum, or constant flexed knee at 3 months after surgery * Informed consent not obtained

Design outcomes

Primary

MeasureTime frameDescription
Change in passive hamstring stiffnessACLR group: Two evaluations on both injured and healthy knees: (1) 4 months after surgery and (2) 8 months after surgery; Control group:one evaluation at a single point in time through study completion (an average of one year)Measurement of knee flexors stiffness (in newton.meter per degree, Nm/°) on isokinetic dynamometer.
Change in StrengthACLR group: Two evaluations on both injured and healthy knees: (1) 4 months after surgery and (2) 8 months after surgery; Control group:one evaluation at a single point in time through study completion (an average of one year)Measurement of knee extensors and flexors peak strength (in newton.meter, Nm) on isokinetic dynamometer.

Secondary

MeasureTime frameDescription
Individual characteristicsACLR group: Two follow-up medical consultations: (1) 4 months after surgery and (2) 2 years after the surgery for return to sport and reinjury; Control group:one evaluation at a single point in time through study completion (an average of one year)Personal characteristics recorded in the medical report as age, gender, type of sport and sport level of practice and return to sport after the surgery and severe reinjury on the operated knee or contralateral knee.
Surgery characteristicsACLR group only: one follow-up medical consultations at 4 months after surgerySurgery characteristics recorded in the medical report as the type of surgery, the surgery duration and tourniquet time

Countries

France

Outcome results

None listed

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