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Clinical Trials/NCT04233125
NCT04233125
Completed
Phase 1

A Randomized Controlled Trial of Core Decompression With or Without Cement Packing for Osteonecrosis of the Femoral Head - Long Term Results

University of Minnesota0 sites37 target enrollmentJanuary 1, 1997
ConditionsOsteonecrosis

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Osteonecrosis
Sponsor
University of Minnesota
Enrollment
37
Primary Endpoint
Progression Free Survival (PFS)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Osteonecrosis of the femoral head (ONFH) is difficult to treat as collapse frequently occurs after core decompression (CD). This may be due to the failure to provide structural support during revascularization and healing. Reports of polymethylmethacrylate (PMMA) packing of the femoral head after CD for ONFH have noted favorable results. This study was undertaken to determine whether the addition of PMMA packing to CD provides any benefit to progression-free survival (PFS) and conversion to total hip arthroplasty-free survival (CFS). Secondary objectives were to assess for differences in functional outcomes and predictive factors for progression of the disease.

Detailed Description

A prospective randomized controlled trial comparing the results of CD vs. CD + PMMA packing in pre-collapse ONFH was set up. Consecutive symptomatic patients aged \>14 years with Association Research Circulation Osseous (ARCO) Stage I and II ONFH diagnosed using MRI and radiographic imaging were enrolled in this study. Exclusion criteria were pre-existing collapse, sub-chondral fracture or degenerative changes of the hip. After obtaining informed written consent, patients are asked to complete the Harris Hip Score (HHS), Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), and a health status questionnaire Short Form-36 (SF-36). The femoral heads enrolled into the study are randomized using a computer-generated card draw system to one of following: core decompression (CD) or core decompression with PMMA cement packing (CD + PMMA). Allocation concealment was practiced with the use of opaque envelopes. Patients with bilateral involvement who had been randomized to one treatment modality for one femoral head were automatically selected to receive the other treatment modality for the contralateral femoral head. Blinding of either surgeon or patient is impossible. The patients were followed up after surgery every 3-4 months for the first 2 years after which the patients were seen annually. Completed questionnaires and radiographs were obtained at each visit. Statistical Analysis The date of index procedure (CD or CD + PMMA) was used as start date for the purpose of statistical analysis. Progression Free Survival was defined as the time to radiographic progression and Conversion Free Survival (CFS) as the time to a THA. In case of patients who did not have radiographic progression, the date of their last follow up or death was used for the analysis. The SAS software will be used for all the analyses. The Log rank and Gerhan-Wilcoxon tests were used to compare Kaplan-Meier survival curves for the time from the date of the index procedure to radiographic progression (subchondral collapse) or conversion to THA for separate groupings based on age at index procedure (\<40 , \>40 yrs), smoking (Y/N), location (central, medial, lateral), percent involvement (\<15% \[mild\], 15% to 30% \[moderate\], or \>30% \[severe\]), index of necrotic extent (\<40 or \>40), and modified index of necrotic extent (\<40 or \>40). Whenever factors were found to affect the survival curves mainly in the initial year the Gerhan-Wilcoxon test was used as the test of significance. The Kaplan-Meier curves were also compared for the main cohorts of CD vs. CD + PMMA. Cox proportional hazards regression was used to compare factors (age, smoking, location, percent involvement, index of necrotic extent, and modified index of necrotic extent) with regards to their ability to predict the time to progression or revision to THA. Mixed multilevel regression modeling was used to test for group differences in the change in self-rated health survey scores over time from baseline over the post-operative period. The hierarchical linear modeling approach has a number of advantages over traditional repeated measures approaches for modeling change over time, including allowance for missing data and for varying measurement times across subjects. Separate models were generated for SF-36, Harris Hip Score and WOMAC scores over two-year and over 5-year post-operative time periods.

Registry
clinicaltrials.gov
Start Date
January 1, 1997
End Date
January 1, 2008
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Association Research Circulation Osseous (ARCO) Stage I and II ONFH diagnosed using MRI and radiographic imaging

Exclusion Criteria

  • pre-existing collapse, subchondral fracture or degenerative changes of the hip

Outcomes

Primary Outcomes

Progression Free Survival (PFS)

Time Frame: 5 years

Progression Free Survival (PFS) is defined as the length of time (reported in months) following surgery that participants have no signs of radiographic progression of femoral head osteonecrosis. Radiographic progression is defined as any degree of flattening or loss of spherical contour of the femoral head as detected on the radiographs or MRI. Appearance of a subchondral fracture (crescent sign) on radiographs or MRI was also considered a sign of progression.

Secondary Outcomes

  • Change in Harris Hip Score (HHS)(baseline, 2 years post surgery)
  • Change in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)(baseline, 2 years post surgery)
  • Conversion Free Survival (CFS)(5 years)
  • Change in Short Form-36 (SF-36)(baseline, 2 years post surgery)
  • Mean Harris Hip Score (HHS)(baseline, 2 years post surgery, 5 years post surgery)
  • Mean Short Form-36 (SF-36)(baseline, 2 years post surgery, 5 years post surgery)
  • Mean Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)(baseline, 2 years post surgery, 5 years post surgery)

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