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ACL ReconstructionNCT03081026

Transphyseal Vs. Physeal Sparing ACL Reconstruction in Skeletally Immature Patients: Risk of Subsequent Lower Extremity Growth Deformity

An observational study of ACL Reconstruction, run by Duke University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

To assess the risk of lower extremity angular growth deformity following anterior cruciate ligament (ACL) reconstructions in young patients who are not yet skeletally mature. The study will compare two surgical techniques (physeal sparing vs transphyseal). Read more about this study

Who is it for?
Ages 6 to 16 years
Conditions the study is for
ACL Reconstruction
What is being tested?
Bilateral hip to ankle x-ray, exam and strength testing.
How many people
49 participants
Where
1 siteUnited States
Study dates
1 May 2017to 6 Mar 2020
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 16 years
  • All sexes
  • No healthy volunteers
  • Child

Study population: Single site patients of five orthopaedic sports medicine attendings who had an ACL reconstruction between the ages of 6-16 with open physes in the time interval from January 1, 2005-December 31, 2016.

Who may be able to join

  • Subjects will be identified by reviewing medical records that include a procedure code for ACL reconstruction in patients between the ages of 6-16 at the time of surgery. Patients meeting the inclusion criteria will be contacted by phone and invited to participate in the study. A key personnel member who is part of the principal investigator's research staff will make phone contact with the patient. The study will be explained and any questions that the subject may have will be answered at that time. If the subject agrees to participate in the study, he/she will make an appointment at that time to come in to be consented and participate in the study and for imaging and testing at Duke Sports Sciences Institute.

Who cannot join

  • Pregnant Females

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Duke Sports Science Institute

    Durham, North Carolina, 27705

Other trials in United States

About this study

To assess the risk of lower extremity angular growth deformity following anterior cruciate ligament (ACL) reconstructions in young patients who are not yet skeletally mature. The study will compare two surgical techniques (physeal sparing vs transphyseal).

Read the detailed description

Background \& Significance: In the adult population, the vast majority of ACL reconstructions are performed by drilling femoral and tibial bone tunnels. Because these patients have achieved physeal closure by the time of surgery, there is no risk of angular growth deformity when creating tibial and femoral tunnels. However, in the pediatric patient with open tibial and femoral physes, there is concern that drilling across the physes using standard tunnels may cause physeal injury with resultant angular deformity. Other surgical techniques have been described that allow the graft to be placed without drilling tunnels across the tibial and femoral physes but there is debate regarding whether or not these "physeal sparing" techniques are as effective as the transphyseal tunnel positions. Drilling the tunnels in the epiphysis to avoid the physis is a common "physeal sparing" technique. It is debated whether this technique could also cause growth disturbances. Given the increasing number of pediatric ACL injuries and that 95% of patients age 12 or less have open physes and that 94% of patients age 14 or greater have closed physes, this topic is of significant interest. Similar studies have been conducted but most have been either small and underpowered or have included older adolescent patients. At Duke Sports Sciences Institute, we have a sizable population of patients age 16 or less who have undergone ACL reconstruction with both transphyseal and all epiphyseal techniques. This provides a unique opportunity to analyze and compare these two groups with respect to clinical outcome and the incidence of growth disturbance or angular deformity

Design \& Procedures: The investigator will conduct a review of medical records of seven providers at a single site institution to determine the subject population. Specifically, the investigator will look for patients who had an ACL reconstruction between the ages of 6-16 after January 1, 2005. The investigator will confirm in the medical record and in pre-operative radiographs that the growth plates were open at the time of surgery. Only subjects with open physeal will be enrolled in the study and they will be placed in 3 cohorts: Ages less than 12, 12-13, and 14 - 16. Subjects will be contacted by phone by a member of the team and asked to return to Duke Sports Sciences Institute to participate in the study. Upon arrival to clinic, subjects will be consented for the study and undergo a full physical exam - specifically targeting the gait and range of motion, as well as the Lachman, Anterior Drawer and Pivot Shift maneuvers to assess stability and functionality of the graft. In addition, they will complete a questionnaire designed to elicit patient satisfaction and level of activity/sports participation after the initial recovery period. Bilateral hip to ankle radiographs will be taken of each subject. These radiographs will be analyzed to assess for any angular deformity between the surgical and non-surgical leg. In addition, baseline knee x-rays will be reviewed for determination of skeletal maturity at time of injury/surgery. Data will be organized according to patients who underwent transphyseal reconstruction and patients who underwent physeal sparing reconstruction and separated into the corresponding age group. Comparisons will be made between the two surgical techniques based on the following criteria:

  • Patient satisfaction and return to function
  • Graft stability
  • Angular deformity
  • Skeletal maturity at the time of surgery

Study Interventions: Subjects will undergo physical examination (gait, inspections, range of motion and instability testing) and completion of an outcome tool survey (IKDC score/PediIKDC, VAS, Marx, and ACL-RSIsurvey). Subjects will undergo bilateral hip to ankle radiographic imaging to assess for growth deformity. Subjects will also be asked to give their permission to review their medical record and imaging pertinent to the knees and knee surgery.

Data Analysis \& Statistical Considerations: Patient's data will be collected in a database program, indexed initially by medical record number. After case collection, case numbers will be applied and medical record numbers stripped from the data. The code linking medical record number to case number will be kept in a locked file with access limited to primary investigator.

Contingency analysis using the Fisher exact test will be used to compare the distribution of normal/nearly normal exam findings between the three cohorts

Descriptive statistics (mean, standard deviation and range) will be reported for each of these scores

Scores will be compared between the three cohorts using ANOVA with post-hoc analysis using Tukey's correction for multiple comparisons

Privacy, Data Storage \& Confidentiality: The primary investigator will collect data in a computerized database using a commercially available database program. During collection, data will be indexed by the patient's medical record number. After data collection, a case number will be assigned to the data and the medical record number (the only identifying data collected) will be stripped from the database. The code linking medical record number to case number will be kept in a locked file with access limited to primary investigator. When the study is complete the code linking medical record numbers to case numbers will be destroyed. During data collection and review, protected health information will be available only to the primary investigator and will not be reused or disclosed to any other person or entity, except as required by law, for authorized oversight of the research study.

Being tested
Bilateral hip to ankle x-ray, exam and strength testing.
Keywords
surgery, ages 6-16

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Bilateral hip to ankle x-ray, exam and strength testing.Diagnostic test

    Only an X-Ray is performed and reviewed to identify any growth disturbances.

Study groups in NCT03081026
Study groupRoleWhat they receive
Ages less than 12Those having ACL Reconstruction surgery during the desired dates at age 12 or less.
Receives: Diagnostic Test: Bilateral hip to ankle x-ray, exam and strength testing.
Ages 12-13Those having ACL Reconstruction surgery during the desired dates at ages 12 and 13.
Receives: Diagnostic Test: Bilateral hip to ankle x-ray, exam and strength testing.
Ages 14 - 16Those having ACL Reconstruction surgery during the desired dates at ages 14 - 16.
Receives: Diagnostic Test: Bilateral hip to ankle x-ray, exam and strength testing.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Limb length discrepancy

    Bilateral hip to ankle radiographs measurements.

    Measured: Clinic visit, approximately 1 hour

  2. Limb Angular alignment

    Bilateral hip to ankle radiographs measurements

    Measured: Clinic visit, approximately 1 hour

Secondary outcomes (1)
  1. Range of motion measurements

    Each patient will be examined and measures of knee range of motion with a goniometer, Lachman and pivot shift will be performed. The Lachman and pivot shift will be dichotomized into two groups: normal/nearly normal and abnormal/severely abnormal.

    Measured: Clinic visit, approximately 1 hour

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Mar 2017
  2. Study start1 May 2017
  3. Primary completion6 Mar 2020
  4. Study completion6 Mar 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
49 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03081026
Sponsor's protocol ID
Pro00063612
Status last verified
Oct 2020
First submitted
8 Mar 2017
Last updated
8 Oct 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: De-identified data will be sent to SmithNephew

Questions about this trial

What is this clinical trial studying?

An observational study of ACL Reconstruction, run by Duke University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Oct 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Limb length discrepancy (time frame: Clinic visit, approximately 1 hour). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Oct 2020.

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