Actively Recruiting

Age: 18Years +
All Genders
NCT06921889

The Biomechanical Outcomes of Autologous Chondrocyte Implantation

Led by University of Manchester · Updated on 2026-05-07

47

Participants Needed

7

Research Sites

116 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Injury to the knee can damage the lining of the knee's bones, called cartilage. Cartilage injuries cause pain and limit movement, making activities like walking, playing sports, and working difficult. Cartilage cannot repair itself well, so surgery is often needed to repair it. People who have cartilage repair surgery want to return to normal activities after their operation. Doctors and scientists know the operation can reduce pain, but do not fully understand how it affects movement. This research will help us see if knee function gets better after cartilage repair surgery. The results will help doctors and patients understand what to expect from the surgery. It could also uncover common problems after surgery that could be fixed with physiotherapy. This research is important because untreated cartilage injuries can develop into arthritis later in life. Arthritis is a painful lifelong condition that could be prevented by effectively treating the cartilage injury. In this study, adult patients who are waiting to have a type of cartilage repair surgery called 'autologous chondrocyte implantation' (ACI) at one of 7 hospitals will be invited to take part in the study by their surgeon. Patients who decide to take part will be invited to two appointments at their own hospital, where assessments of their knee function will be performed. The tests will assess the knee's movement, and the patient's balance and walking abilities. The first research appointment will take place before the operation, and the second and final appointment will take place 6-months after surgery. The results of this study will help us understand how knee function changes after cartilage repair surgery. The study will take place across 7 ACI centres in England, and is funded by Orthopaedic Research UK and the British Association for Surgery of the Knee.

CONDITIONS

Official Title

The Biomechanical Outcomes of Autologous Chondrocyte Implantation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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 a chondral injury by a consultant orthopaedic surgeon
  • Over 18 years old and able to provide informed consent
Not Eligible

You will not qualify if you...

  • Listed for any treatment other than autologous chondrocyte implantation (ACI) surgery
  • Under 18 years old and unable to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

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Research Team

G

Gwenllian F Tawy, PhD

CONTACT

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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