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

NCT01754298 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 91

Last updated 2020-12-03

No results posted yet for this study

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.

Conditions

  • Juvenile Osteochondritis Dissecans

Interventions

PROCEDURE

Retro-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.

PROCEDURE

Trans-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 & Collaborators

  • Pediatric Orthopaedic Society of North America

    collaborator OTHER
  • University of Pennsylvania

    collaborator OTHER
  • Tennessee Orthopedic Alliance

    collaborator OTHER
  • Children's Hospital Medical Center, Cincinnati

    collaborator OTHER
  • Children's Hospital and Health System Foundation, Wisconsin

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • The Hospital for Sick Children

    collaborator OTHER
  • Children's Hospital of Philadelphia

    collaborator OTHER
  • Kaiser Permanente

    collaborator OTHER
  • Rady Children's Hospital, San Diego

    collaborator OTHER
  • St. Luke's Children's Hospital

    collaborator OTHER
  • Medical College of Wisconsin

    collaborator OTHER
  • Connecticut Children's Medical Center

    collaborator OTHER
  • Hospital for Special Surgery, New York

    collaborator OTHER
  • Boston Children's Hospital

    lead OTHER

Principal Investigators

  • Benton Heyworth, M.D. · Boston Children's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
8 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-18
Primary Completion
2019-07-29
Completion
2020-10-16

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01754298 on ClinicalTrials.gov