Randomized Evaluation of BST-CarGel Versus Microfracture Alone On Recovery From Distal Femoral Cartilage Lesions (RECORD)

This multi-centre randomized, controlled trial will assess the impact of BST-CarGel scaffold with microfracture versus microfracture alone on short and long term clinical benefit in patients with cartilage lesions of the femoral condyle requiring operative management.

Study Overview

• Status: Terminated
• Conditions: Degenerative Lesion of Articular Cartilage of Knee; Traumatic; Lesion
• Intervention / Treatment: Procedure: Microfracture treatment; Device: BST-CarGel

Detailed Description

The current standard of treatment for cartilage lesions on the femoral condyle is microfracture, which is conducted by penetrating the subchondral bone below the lesion. This procedure creates a natural healing response as a result of the bleeding and clotting caused by the microfracture, restoring the lesion. BST-CarGel (Piramal Life Sciences, Bio-Orthopaedic Division), a liquid chitosan-containing polymer scaffolding, has been developed as an intra-articular injectable scaffold to aid in the stabilization of the blood clot created by microfracture. BST-CarGel does not interfere with the normal clotting process; however, it enables a prolonged healing time due to the increased stabilization of the clot within the lesion and the inhibition of clot retraction.

The RECORD trial is a multi-centre, randomized, controlled trial to assess the impact of the BST-CarGel scaffold and microfracture versus microfracture alone on short term clinical benefit as measured by loaded knee pain (single leg squat) on a visual analogue scale (3-6 months), mid-long term clinical benefit as measured by the same loaded knee pain (single leg squat) (9, 12, and 24 months) and Tegner Activity Score (TAS), International Knee Documentation Committee (IKDC), and Knee Injury and Osteoarthritis (KOOS) at 3, 6, 9, 12 and 24 months post-operatively. Approximately 158 participants with full-thickness grade III and IV cartilage lesions will be randomised in a 1:1 ratio to receive one of the two treatments during an arthroscopic procedure and will be followed for up to 24 months to collect outcomes.

• Study Type: Interventional
• Enrollment (Actual): 5
• Phase: Phase 4

Contacts and Locations

Study Locations

• Australia
  • Adelaide, Australia, 5000
    • Calvary Wakefield Hospital
  • Murdoch, Australia, 6150
    • Murdoch Orthopaedic Clinic
• Canada
  • Banff, Canada, T1L1B3
    • Banff Sport Medicine
  • London, Canada, N6A3K7
    • Fowler Kennedy Sport Medicine Clinic
  • Montreal, Canada, H1T4B3
    • Hôpital Maisonneuve-Rosemont
• France
  • Lyon, France, 69004
    • Hôpital de la Croix-Rousse
  • Nancy, France, 54000
    • CHRU Nancy - Hospital Central
• Germany
  • Regensburg, Germany, 93042
    • University Medical Centre Regensburg
• Spain
  • Barcelona, Spain, 08035
    • Hospital Universitari Vall d'Hebron
  • Barcelona, Spain, 08023
    • Hospital Quironsalud Barcelona
  • Barcelona, Spain, 08003
    • Hospital Universitari del Mar
  • Zaragoza, Spain, 50009
    • Hospital Universitario Miguel Servet
• Switzerland
  • Zurich, Switzerland, 8032
    • SportClinic Zurich / Hirslanden Clinic
• United Kingdom
  • Birmingham, United Kingdom, B312AP
    • The Royal Orthopaedic Hospital
  • Southampton, United Kingdom, S0166YD
    • University Hospital Southampton

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 55 years (ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• requires cartilage repair treatment due to distal femoral cartilage lesion
• is 18-55 years of age at the time of surgery
• has single, focal cartilage lesion on one of the femoral condyles
• has symptomatic cartilage lesion that has failed conservative management
• has a single lesion classified as focal, full-thickness grade 3 or 4 according to the ICRS (3A, 3B, 3C, 3D and 4A)
• an area of lesion between 1.5-3 cm2 after debridement
• has a stable knee (<5-mm side-to-side difference on Lachman and varus and valgus stress testing and grade 0 or 1 on the pivot-shift test) and an intact meniscal rim
• is willing and able to participate in required follow-up visits at the investigational site and to complete study procedures and questionnaires and recommended physiotherapy regimen
• has agreed to discontinue the use of all knee pain medication 3 days before the pre-treatment visit and the post-treatment follow-up visits at 3, 6, 9, 12, and 24 months
• has consented to participating in the study by signing the IRB/EC approved informed consent form
• no deep osteochondral defect ( < 5 mm bone loss)

Exclusion Criteria:

• has multiple lesions or kissing (opposing) lesion(s) greater than GII
• has clinically relevant compartment malalignment (>5°)
• has bone cyst(s) associated with, or adjacent to, the index lesion
• has Osteochondritis Dissecans with bone or bone-cartilage fragment in place
• has had ligament treatments in the index knee within the previous 24 months
• has had surgical cartilage treatments in the index knee within previous 12 months
• has had intra-articular injections in the index knee within the previous 2 months
• has diagnosis of an immunosuppressive disorder
• has a BMI > 30 kg/m2
• has concomitant healing bone fractures
• has a single lesion classified as focal, full-thickness grade 4B as defined by ICRS
• has noteworthy pain in the ipsilateral hip or ankle or contralateral hip, knee, or ankle
• has inflammatory arthropathy
• has blood clotting disorders, was receiving anticoagulant therapy, or has recurring deep vein thrombosis
• has a serious heart condition or liver and/or renal abnormalities diagnosed within the previous 24 months
• has chronic infection of the lower joint extremities
• has a history of alcohol or drug abuse within the previous 12 months
• is facing current or impending incarceration
• has a known allergy to shellfish
• is pregnant or plans to become pregnant during the course of the study
• in the opinion of the PI, has an emotional or neurological condition that would pre-empt their ability or willingness to participate in the study including mental illness, drug or alcohol abuse
• chronic knee pain
• has a documented medical history of vitamin-D deficiency that is not being managed with supplementation
• is entered in another investigational drug, biologic, or device study or has been treated with an investigational product in the past 30 days
• requires an open procedure
• is known to be at risk for lost to follow-up, or failure to return for scheduled visits

Study Plan

How is the study designed?

Design Details

• Primary Purpose: BASIC_SCIENCE
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: SINGLE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
ACTIVE_COMPARATOR: Microfracture treatment; Microfracture surgery of the femoral condyle	Procedure: Microfracture treatment; Microfracture is performed by penetrating the subchondral bone beneath the cartilage lesion inducing a bleeding response.
EXPERIMENTAL: BST-CarGel plus microfracture treatment; BST-CarGel combined with fresh, autologous whole blood and applied to the lesion on the femoral condyle with a syringe following an arthroscopic microfracture surgery.	Procedure: Microfracture treatment; Microfracture is performed by penetrating the subchondral bone beneath the cartilage lesion inducing a bleeding response.; Device: BST-CarGel; BST-CarGel is combined with fresh, autologous whole blood and applied to the lesion on the femoral condyle with a syringe following microfracture arthroscopic surgery.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in loaded knee pain (single leg squat) visual analogue scale (VAS)	Used to demonstrate patient clinical improvement. The VAS is one of the most commonly used measures of pain intensity, where the patient rates their pain on a scale from 0 to 10 (0=no pain; 10=maximum pain possible).	Baseline to 24 months post-surgery
Change in knee function measured by the TAS questionnaire	The TAS is a validated patient-administered questionnaire for use in multiple knee injuries and consists of a numerical scale ranging from 0 to 10 to indicate the ability to perform specific activities.	Baseline to 24 months post-surgery
Change in knee function measured by the IKDC questionnaire	The IKDC measures the progress in symptoms, function, and sports activities caused by knee impairment after a treatment has been performed. It can be used with reliability and validity in patients with a range of knee conditions.	Baseline to 24 months post-surgery
Change in knee function measured by the KOOS questionnaire	The KOOS is a measure of a patient's perceived knee pain and function, as well as associated problems with their knee status. It contains 42 items that are all recorded on a five-point Likert Scale by the patient.	Baseline to 24 months post-surgery

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Repair tissue quantity and quality	Measured by MOCART Score and percentage lesion fill. The MOCART Score will be completed by two independent, blinded, well-trained radiologist readers.	Up to 24 months post-surgery
Adverse events related to treatment		Up to 24 months post-surgery
Economic evaluation	Measured by study-specific Resource Utilization Questionnaires which will be used to determine the costs associated with the use of the BST-CarGel scaffold treatment.	surgical visit, 2 weeks, 6 weeks, 3 months, 6 months, 9 months,12 months and 24 months post-surgery

Collaborators and Investigators

• Sponsor: Piramal Healthcare Canada Ltd
• Collaborators: Smith & Nephew, Inc.; Global Research Solutions
• Investigators: Study Chair: Jean-Pierre Desmarais, Piramal Healthcare Canada Ltd

Publications and helpful links

General Publications

• Shive MS, Stanish WD, McCormack R, Forriol F, Mohtadi N, Pelet S, Desnoyers J, Methot S, Vehik K, Restrepo A. BST-CarGel(R) Treatment Maintains Cartilage Repair Superiority over Microfracture at 5 Years in a Multicenter Randomized Controlled Trial. Cartilage. 2015 Apr;6(2):62-72. doi: 10.1177/1947603514562064.
• Stanish WD, McCormack R, Forriol F, Mohtadi N, Pelet S, Desnoyers J, Restrepo A, Shive MS. Novel scaffold-based BST-CarGel treatment results in superior cartilage repair compared with microfracture in a randomized controlled trial. J Bone Joint Surg Am. 2013 Sep 18;95(18):1640-50. doi: 10.2106/JBJS.L.01345.

Study record dates

Study Major Dates

• Study Start (ACTUAL): July 26, 2017
• Primary Completion (ACTUAL): March 6, 2018
• Study Completion (ACTUAL): March 6, 2018

Study Registration Dates

• First Submitted: November 21, 2016
• First Submitted That Met QC Criteria: November 30, 2016
• First Posted (ESTIMATE): December 5, 2016

Study Record Updates

• Last Update Posted (ACTUAL): November 1, 2018
• Last Update Submitted That Met QC Criteria: October 30, 2018
• Last Verified: August 1, 2017

More Information

Terms related to this study

• Keywords: Microfracture; Cartilage Repair; Bone Marrow Stimulation; BST-CarGel; Cartilage Lesion, Chondral Lesion; Femoral condyle; Tear of Articular Cartilage of Knee, Current
• Additional Relevant MeSH Terms: Fractures, Bone; Wounds and Injuries; Fractures, Stress
• Other Study ID Numbers: BST-CarGel Pr001

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No