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Study of Two Surgical Drilling Techniques to Treat Juvenile Osteochondritis Dissecans of the Knee

Retro Versus Trans Articular Drilling for Juvenile Osteochondritis Dissecans of the Knee: A Multicenter, Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01754298
Enrollment
91
Registered
2012-12-21
Start date
2013-01-18
Completion date
2020-10-16
Last updated
2020-12-03

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

Conditions

Juvenile Osteochondritis Dissecans

Keywords

osteochondritis dissecans (OCD), juvenile osteochondritis dissecans (JOCD), knee osteochondritis dissecans, retro-articular drilling, trans-articular drilling, stable osteochondritis dissecans lesion

Brief summary

The purpose of this study is to compare the functional, clinical and radiographic outcomes associated with trans-articular drilling versus retro-articular drilling, two commonly employed techniques of operative treatment for stable forms of juvenile osteochondritis dissecans (JOCD) lesions. This study also aims to better define the natural history of this condition in its most commonly identified pathological state (as a stable lesion) following surgical intervention by determining the rate of radiographic healing and any need for secondary surgery.

Interventions

PROCEDURERetro-articular drilling

* Drilling must be performed under AP and lateral fluoroscopic guidance, with no additional drilling in 'trans-articular', or intra-articular trans-condylar fashion. * Use a 0.045 K-wire for drilling. * Minimum of 8 wire passes per square centimeter with no maximum number of wire passes.

PROCEDURETrans-articular drilling

* Drilling must be performed, under arthroscopic visualization, directly through the articular cartilage, with no additional drilling in 'retro-articular', 'extra-articular', or trans-condylar (through the intercondylar notch) * Use a 0.045 K-wire for drilling * A minimum 4 wire passes per square centimeter, with a maximum of 5 wire passes per square centimeter

Sponsors

Pediatric Orthopaedic Society of North America
CollaboratorOTHER
University of Pennsylvania
CollaboratorOTHER
Tennessee Orthopedic Alliance
CollaboratorOTHER
Children's Hospital Medical Center, Cincinnati
CollaboratorOTHER
Children's Hospital and Health System Foundation, Wisconsin
CollaboratorOTHER
Washington University School of Medicine
CollaboratorOTHER
The Hospital for Sick Children
CollaboratorOTHER
Children's Hospital of Philadelphia
CollaboratorOTHER
Kaiser Permanente
CollaboratorOTHER
Rady Children's Hospital, San Diego
CollaboratorOTHER
St. Luke's Children's Hospital
CollaboratorOTHER
Medical College of Wisconsin
CollaboratorOTHER
Connecticut Children's Medical Center
CollaboratorOTHER
Hospital for Special Surgery, New York
CollaboratorOTHER
Boston Children's Hospital
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Diagnosis of JOCD, * Lesion located on the lateral aspect of the medial femoral condyle, * Lesion considered stable based on MRI, * Patient deemed skeletally immature based on MRI, * Completed a course of conservative therapy.

Exclusion criteria

* Significant concomitant knee pathology (AVN, fracture, inflammatory arthritis, ACL tear, discoid/meniscal tear, etc.) * Lesion healed sufficiently and surgery is not recommended, * Prior surgery on the affected knee, * Diagnosis of metabolic bone disorder (e.g. osteogenesis imperfecta), * Diagnosis of sickle cell disease, * History of prolonged corticosteroid or chemotherapy treatment,

Design outcomes

Primary

MeasureTime frame
Physical functioning measured by the Pedi-IKDC (International Knee Documentation Committee) total scoreOne year post-surgery

Secondary

MeasureTime frameDescription
Activity level as measured by the Marx Activity ScaleOne year post-surgery
Physical functioning as measured by the Pedi-IKDC total scoreTwo years post-surgery
Time to lesion healing3 months to 2 years post-surgeryLesion healing will be assessed by x-ray at multiple time points

Other

MeasureTime frameDescription
Surgical complications1 week to 1 year post-surgeryInadvertent displacement of OCD fragment; damage to articular cartilage and physes

Countries

Canada, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026