Actively Recruiting
Investigating the Biomechanical and Functional Outcomes of Autologous Chondrocyte Implantation for Knee Cartilage Injuries: A Multi-centre Study
Led by University of Manchester · Updated on 2026-05-07
47
Participants Needed
7
Research Sites
N/A
Total Duration
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AI-Summary
What this Trial Is About
Knee cartilage injuries can cause pain and limit movement, affecting daily activities like walking and sports. Since cartilage heals poorly on its own, surgery such as autologous chondrocyte implantation (ACI) is often needed. This study aims to understand how knee function changes after ACI surgery, helping doctors and patients know what to expect and identify issues that physiotherapy might improve. The research is important because untreated cartilage damage can lead to arthritis, a painful condition later in life. Participants in this study will all undergo ACI surgery, which involves two procedures: first, harvesting cartilage cells from the patient, then growing these cells in a lab before implanting them to repair the knee's damaged cartilage. The study will take place at seven hospitals, with patients invited to attend two appointments at their hospital—one before surgery and one six months after—to assess knee function. During these visits, researchers will measure knee range of motion using a goniometer and analyze walking patterns using motion capture technology. They will also evaluate balance and walking ability. The study's results will provide detailed information about knee movement and function after ACI surgery, which could help improve patient care and treatment outcomes. The entire participation spans about six months with assessments before and after surgery.
CONDITIONS
Brief Title
The Biomechanical Outcomes of Autologous Chondrocyte Implantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of a chondral injury to the knee by a consultant orthopaedic surgeon
- Listed for autologous chondrocyte implantation (ACI) surgery for the chondral injury
- Age 18 years or older
You will not qualify if you...
- Scheduled for any treatment other than autologous chondrocyte implantation (ACI)
- Under 18 years old
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Procedure plus immediate recovery period
Participants undergo autologous chondrocyte implantation (ACI), a two-stage surgical procedure to repair damaged knee cartilage. This includes cell harvesting, laboratory expansion, and implantation of chondrocytes into the knee.
1 to 2 visits related to surgery and immediate post-operative care
Duration - Up to 6 months
Participants are monitored to assess knee range of motion and gait biomechanics outcomes after ACI surgery.
Multiple follow-up visits over 6 months for functional and biomechanical assessments
Trial Site Locations
Total: 7 locations
1
Royal Orthopaedic Hospital
Birmingham, United Kingdom, B31 2AP
Not Yet Recruiting
2
Addenbrooke's Hospital
Cambridge, United Kingdom, CB2 0QQ
Not Yet Recruiting
3
Chapel Allerton Orthopaedic Centre
Leeds, United Kingdom, LS7 4SA
Actively Recruiting
4
Trafford General Hospital
Manchester, United Kingdom, M415SL
Actively Recruiting
5
Southampton General Hospital
Southampton, United Kingdom, SO16 6YD
Not Yet Recruiting
6
Royal National Orthopaedic Hospital
Stanmore, United Kingdom, HA7 4LP
Actively Recruiting
7
New Cross Hospital
Wolverhampton, United Kingdom, WV10 0QP
Actively Recruiting
Research Team
G
Gwenllian F Tawy, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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