Evaluation of Subchondroplasty™ for Defects Associated With Bone Marrow Lesions

Bone Marrow Edema Clinical Trial

— SCP  

Official title:

Prospective Efficacy Evaluation of Subchondroplasty™ for the Treatment of Defects Associated With Tibial Bone Marrow Lesions

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01621893
• Other study ID #: KC-SCP-001
• Status: Completed
• Start date: March 26, 2012
• Est. completion date: May 26, 2021

Study information

• Verified date: September 2021
• Source: Zimmer Biomet
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Studying long-term changes in a sub-set of patients who undergo the Subchondroplasty procedure including changes in pain, function, and overall health.

Description:

This study is designed as a prospective, consecutive series outcomes study. Patients presenting with knee pain associated with bone marrow lesions that meet the inclusion criteria will be eligible to undergo Subchondroplasty procedure. The subjects will be followed for twenty-four (24) months after surgery via office visits and will be contacted once per year for up to 5 years post-operatively and asked questions regarding their pain and functioning to further understand long-term outcomes.. Seventy (70), a ( minimum of sixty-two (62)) patients who meet the inclusion/exclusion criteria will be enrolled in the study. Up to 5 sites will participate in this study. The study is intended to provide an estimate of one-year and two-year clinical success with minimum bias and with sufficient statistical precision to permit meaningful comparison to commonly accepted two-year clinical success rates for currently available treatment alternatives. An improvement of 10 points on the Knee Injury and Osteoarthritis Outcome Score (KOOS) Pain Subscore on the KOOS Scoring System from baseline to 1-year post-operative is considered minimal perceptible clinical improvement and will be used to define the primary clinical success criterion for this study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: May 26, 2021
• Est. primary completion date: January 17, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 70 Years

Eligibility

Inclusion Criteria:

• Subject is 40-70 of age and skeletally mature

• Subject BMI is < 40

• Subject has experienced pain in knee for at least 3 months

• BML is confirmed on T2 weighted MR Imaging by presence of white signal

• Subject has single BML of tibia, single BML of femur, or adjoining BML's of tibia & femur

• Baseline KOOS pain subscore is =65

• Subject's involved knee alignment is defined radiographically as one of the following:

Neutral, = to 7 degrees mechanical varus or < 7.5 degrees mechanical valgus

• Subject's ACL and PCL ligaments are intact

• Subject has failed no more than one operative treatment on treatment knee, and none within 6 months prior to enrollment

• Subject is willing and able to sign a written consent form

• The subject has the mental capacity and the willingness to comply with the specified follow-up evaluations, and can be contacted by telephone by the site personnel.

Exclusion Criteria:

• Surgeon deems subject's pain to be primarily related to an alternate condition such as a baker cyst, synovitis, meniscal pathology, or other

• BML caused by acute trauma

• Subject is not neurologically intact (sensory, motor, and reflex deficit)

• Subject is insulin dependent

• Subject has a history of any invasive malignancy (except non-melanoma skin cancer), unless treated with curative intent and with no clinical signs or symptoms of the malignancy for 5 years

• Subject with primary bone tumor in the knee area

• Subject anticipates having a lower extremity surgery other than the investigational surgery during the course of the study

• Subject has a history of substance abuse

• Subject is currently involved in another study or have received investigational product or treatment within the last 30 days

• Subject is pregnant or planning on becoming pregnant during the study period

• Subject is accepting workers' compensation

Related Conditions & MeSH terms

• Bone Marrow Edema
• Edema

Intervention

Procedure:
• Subchondroplasty

Locations

Country	Name	City	State
United States	CORE Orthopaedics	Encinitas	California
United States	Steadman Hawkins Foundation	Greenville	South Carolina
United States	Hinsdale Orthopedics	New Lenox	Illinois
United States	Hospital for Joint Disease	New York	New York
United States	Rothman Institute	Philadelphia	Pennsylvania
United States	Allegheny Orthopaedic Associates	Pittsburgh	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Zimmer Biomet

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Knee Injury Osteoarthritis Outcomes Score (KOOS) Pain Subscore	Post-operative KOOS pain subsection score at 1-Year follow-up is improved by at least 10 points. The KOOS is a validated instrument which measures knee pain and function using five subscales: pain, symptoms, function in daily living, function in sport and recreation, and quality of life. The instrument consists of 42 standardized questions each having 5 point Likert response scale	1 Year
Secondary	Improvement from baseline in KOOS subsection scores	The KOOS is a validated instrument which measures knee pain and function using five subscales: pain, symptoms, activities of daily living (ADL), function in sport and recreation, and quality of life. The instrument consists of 42 standardized questions each having 5 point Likert response scale.	24 Months
Secondary	Improvement in VAS	The VAS is a validated pain scale. Subjects are asked to rate the amount of pain they have experienced with activity (walking, climbing stairs) for the past week by placing a slash through a 100mm line, which bests describes the pain when 0 is no pain and 100 is worst pain imaginable. Study personnel will measure where the subject placed the mark and transcribe this on an eCRF.	24 Months
Secondary	Improvement in Modified Knee Score	Subjects will be asked to complete the Modified Knee Score pre-operatively and at each follow-up visit. The Modified Knee Score is a validated questionnaire composed of 4 questions to evaluate pain and function primarily before and after knee arthroplasty. The score is based on a maximum 100 points with Excellent = 85-100; Good = 70-84; Fair = 60-69; Poor = <60	24 Months
Secondary	Improvement in IKDC	The IKDC Questionnaire is a subjective scale that provides patients with an overall function score. The questionnaire looks at 3 categories: symptoms, sports activity, and knee function. A score of zero is the lowest level of function or highest level of symptoms to 100, highest level of function and lowest level of symptoms.	24 Months
Secondary	Maintenance or improvement in usage (i.e., reduction in usage) of NSAIDs, narcotics, anti-inflammatory medications	Subjects will be asked pre-operatively what medications are taken as part of their knee treatment and at each follow-up visit, medications taken or currently taking as part of their recovery	24 Months
Secondary	Complications or secondary procedures at index site of knee	Incidence of secondary or revision procedures will be recorded	24 Months