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Anterior Cruciate Ligament Reconstruction Made With Hamstring Tendon And Quadriceps Tendon Autografts

Prospective Comparison Of Arthroscopic Anterior Cruciate Ligament Reconstrictions Made With Hamstring Tendon And Quadriceps Tendon Autografts

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04940169
Enrollment
38
Registered
2021-06-25
Start date
2018-07-06
Completion date
2021-03-30
Last updated
2021-06-25

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

Conditions

Anterior Cruciate Ligament Injuries

Brief summary

Anterior cruciate ligament reconstruction (ACLR) is one of the most common procedure all around the world, however optimal graft source for ACLR still remains controversial. Although Quadriceps tendon (QT) is the least used and least studied autograft, it could be an appropriate and good alternative for ACLR. If investigaters use the same surgical technique, and exert the same rehabilitation methods they may have better results than hamstring tendon (HT) autografts.

Detailed description

Investigators enrolled 36 patient and randomized them to different group (HT, QT). at the first evaluation examination findings noted, PROMs (patient reported outcome measurements) questioned, thigh circumference measured, flexor and extensor thigh muscle strength recorded with help of Humac CYBEX Norm (CSMI, 2004) device. After these examinations and preparations all patients operated by the same surgeon who is familiar with both technique. The same surgical technique and fixation method used for both groups. At 1st year follow-up all evaluations PROMs (İKDC,lysholm,VAS) and measurements repeated. Back to the sports rates and postoperative complications compared between HT-QT.

Interventions

PROCEDUREanterior cruciate ligament recontruction

Firstly graft is harvested with help of arthroscopy femoral and tibial tunnels created then graft placed into tunnels

Sponsors

SB Istanbul Education and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

diagnosed primary ACL rupture willing to involve study * lesser than Outerbridge 2 cartilage lesions, non-buckethandle meniscus injuries

Exclusion criteria

more than one ligament injury greater than outerbridge 3 cartilage injury buckethandle meniscus injuries re-ruptures bilateral injuries previous knee surgery any disease affecting muscle strength \-

Design outcomes

Primary

MeasureTime frameDescription
KOOSChange from Baseline score at one year.Simple patient reported questionnaire
lysholmChange from Baseline score at one year.Simple patient reported questionnaire
VASChange from baseline score at one year.Simple patient reported questionnaire
IKDCChange from baseline score at one year.Simple patient reported questionnaire
STRENGTH TESTChange from baseline score at one year.Simple patient reported questionnaire
subjective instability testChange from baseline score at one year.instability measure with help of examinations
thigh circumferenceChange from baseline score at one year.circumference measure
one leg hop testChange from baseline score at one year.ask to participant hop on operated leg

Countries

Turkey (Türkiye)

Outcome results

None listed

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