- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01403207
An Analysis of Potential Sex Differences in Knee Osteoarthritis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The goal of this study is to determine if sex differences can be identified in the knee joint that can contribute to the differences in incidence and severity of knee osteoarthritis observed in men and women, particularly over the age of 50. Recent studies assessing the responses of articular chondrocytes to systemic factors suggest that there are underlying differences in the biochemical and molecular characteristics of male and female cells. It is also known that immune responses differ in males and females, suggesting that there may be important differences in the levels of immune modulators in the joint tissues, including the synovial membrane, the synovial fluid, and the cartilage itself. Responses to the vitamin D metabolite 1_,25(OH)2D3 are upregulated in osteoarthritic cartilage, raising the possibility that males and females differ in their circulating levels of vitamin D, in the content of vitamin D metabolites in the synovial tissues, or in the ability of the cells to respond to this steroid. Similarly, in post-menopausal women, circulating estrogen is reduced relative to testosterone, but it is not known if this might impact the knee. Most importantly, it is not known if potential sex differences can be correlated with severity of disease.
This study is based on the hypothesis that sex differences exist in different tissues of the knee joint, which contribute to the increased incidence and severity of knee osteoarthritis in older women as compared to older men.
To test this hypothesis, the investigators will use tissues and fluids that are normally discarded during the course of total knee replacement surgery to investigate potential sex differences.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Florida
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Jacksonville, Florida, United States, 32224
- Mayo Clinic Jacksonville
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
1. Patient demographics (age, sex, BMI). 2. Clinical background material
- Post menopausal female
List of all medications and supplements
- Use of vitamin D supplements (duration and amount)
- Use of bisphosphonates (past and current)
- Use of estrogen (past and current)
Prior trauma or knee surgery
- Have you ever injured the operative knee so badly that it was difficult for you to walk for at least one week?
- Have you ever had any kind of knee surgery? Please include arthroscopy (where they put a scope in your knee), ligament repair surgery, or a meniscectomy (where they repaired or cut away a torn meniscus or cartilage)?
Prior intraarticular injections
- Steroid
- Hyaluronic acid
- SF 12
- WOMAC
- PASE functional scale
- Pain scale: The 11 question OARSI-OMERACT pain scale will be used. Patients will complete the pain scale within 2 weeks prior to surgery and at 3 months following surgery
- Knee pain map: Patients will complete this within 2 weeks prior to surgery and at 3 months following surgery
- Pressure pain thresholds at knee. This will be completed within 2 weeks prior to the surgery and at 3 months following surgery (see attachment for details) 3. Preoperative blood tests
a. Vitamin D level 25 D3 should be measured 4. Standard preoperative radiographs: AP, lateral, standing flexion AP and patellar sunrise
Exclusion Criteria:
- Patients with inflammatory arthritis
- Patients with osteonecrosis
- Patients with prior upper tibial osteotomy
- Premenopausal women
- Patients under age 65 years, older than 75 years
- Patients who are insulin dependent or diabetic
- Patients with a BMI>30
- Patients with a history of knee infection
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
knee osteoarthritis
Many musculoskeletal conditions are impacted by the chromosomal sex of the patient.
While osteoarthritis (OA) is predominant in men younger than 50 years of age, after age 50 the condition is more prevalent in women, particularly post-menopause.
This has implications for diagnosis and treatment of OA, as well as for joint replacement.
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Many musculoskeletal conditions are impacted by the chromosomal sex of the patient.
While osteoarthritis (OA) is predominant in men younger than 50 years of age, after age 50 the condition is more prevalent in women, particularly post-menopause.
This has implications for diagnosis and treatment of OA, as well as for joint replacement.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To determine if there are sex-differences in different tissues of the knee joint
Time Frame: 1 year
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1 year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Analyze preoperative functional and clinical data to determine if there are differences in Vitamin D levels and gender differences.
Time Frame: 1 year
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Analyze preoperative functional and clinical data to determine if there are differences in Vitamin D levels and gender differences.
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1 year
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Mary I O'Connor, MD, Mayo Clinic Jacksonville, Chair, Orthopedics
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11-001468
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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