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Does Bone Grafting at the Time of Bone-Patellar Tendon-Bone ACL Reconstruction Reduce the Incidence of Post-operative Anterior Knee Pain: A Randomized Controlled Clinical Study

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Hartford Hospital

Status

Enrolling

Conditions

ACL Injury

Treatments

Procedure: Autologous bone grafting
Procedure: Absence of autologous bone grafting

Study type

Interventional

Funder types

Other

Identifiers

NCT04958733
HHC-2021-0113

Details and patient eligibility

About

It is estimated that 48 out of 10,000 people, in the United States, will tear their anterior cruciate ligament (ACL) annually and undergo ACL reconstruction (ACLR). Surgeons have several graft options, surgical techniques, and fixation methods to consider when planning how to reconstruct a patient's ACL. Graft options vary greatly and include allografts and autografts with good evidence that are good choices. Further, autografts include several different specific grafts including; bone-patellar tendon-bone (BPTB), hamstring tendons, and quadriceps tendon. There is no clear consensus on which graft type is superior, as each graft has associated positives and negatives.

Historically, autologous BPTB grafts have been the preferred choice of surgeons given its ability to restore rotational stability for the knee, the robust healing with direct bone-to-bone contact at both ends of the graft, and low failure rates. However, there are drawbacks to ACLR using a BPTB graft. Complications following BPTB graft harvesting include patella fractures, patellar tendon ruptures, increased risk of patellofemoral osteoarthritis, lack of terminal extension, and donor-site morbidity. The majority of these complications are associated with low-risk rates, except for donor-site morbidity which may be prevalent in 37-51% of BPTB graft patients. Donor-site pain can manifest as anterior knee, patellofemoral pain, loss of sensory input, or discomfort with kneeling and can negatively influence subjective as well as objective measures of knee function.

Filling bony defects with bone graft is a procedure that is commonly conducted within orthopedics. However, its use in treating the bony defects caused during BPTB graft harvesting is less common as patella and tibial harvest sites are routinely left unfilled. Significant methodological differences in treatment interventions for the patella harvest site, the tibial harvest site, or both and conflicting results have made it difficult to determine if these treatments have clinical utility. To the best of the investigators' knowledge, there has been no investigation looking at the incidence of donor site morbidity treated with autologous bone grafting of the harvest sites. Therefore, the purpose of this study is to determine if filling the harvest site defect is associated with a lower rate of donor site morbidity and better patient reported functional outcomes compared to patients whose harvest site remains unfilled.

The purpose of this study is to compare the rate of donor site morbidity between patients who have their harvest sites bone grafted with autologous bone (BG) and those whose harvest sites remain unfilled (nBG).

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Males and females
  • 18 years of age and older, with no upper age limit
  • A candidate for primary autologous BPTB ACLR
  • Willing to participate in the study

Exclusion criteria

  • Concomitant ligamentous or chondral injury
  • Prior surgery on the index knee
  • Prior history of anterior knee pain or patellofemoral joint pain on the index knee
  • Outerbridge classification > 2 assessed during arthroscopy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups, including a placebo group

Autologous Bone Grafting
Active Comparator group
Description:
Excess bone obtained from graft preparation and the coring reamer will be used to fill the patellar and tibial donor sites.
Treatment:
Procedure: Autologous bone grafting
Control
Placebo Comparator group
Description:
The control group will have their patellar and tibial defects remain unfilled.
Treatment:
Procedure: Absence of autologous bone grafting

Trial contacts and locations

3

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Central trial contact

Regina O Kostyun, MSEd

Data sourced from clinicaltrials.gov

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