FERARI: Functional Exercise Response on osteoArthritis Relaxation Imaging

Sponsor
Cambridge University Hospitals NHS Foundation Trust (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03657303
Collaborator
(none)
18
1
36.3
0.5

Study Details

Study Description

Brief Summary

Osteoarthritis (OA) is the most prevalent cause of mobility impairment and disability in the elderly. Indications at early stages of OA include decreased organisation of the collagen matrix, loss of proteoglycans and increased hydration. Late-stage joint disease can be diagnosed with X-ray, CT, and conventional MRI, but there are no validated methods to image early changes in cartilage microstructure, which are direly needed in early phase clinical development. Newly developed therapies and evaluation techniques are required at earlier stages of disease to offset the growing numbers and costs of end-stage disease.

MRI can probe soft-tissue with physical measurements that are not available through other methods. Quantitative MRI signal relaxation properties are particularly promising for assessing early changes in the cartilage composition. These relaxation properties are sensitive to water content and cartilage macromolecular structure.

Mechanical joint-loading and exercise affects quantitative MRI through cartilage compression and nonuniform deformation. A study measuring MRI relaxation times and using static joint-loading weights has shown differences between OA and healthy subjects. Cartilage volume, which is expected to be related to these relaxation times, recovers within an hour after exercise in healthy runners, with the menisci lagging in their volume recovery rate. Previous exercise studies have not measured post-exercise cartilage recovery using compositional techniques, such as physiologically-sensitive T1ρ and T2, nor probed compositional responses with OA subjects.

The investigators will examine a single knee of an initial 18 participants with MR. Participants will be drawn from two groups: (1) 12 participants aged 40-60 years old with clinical and x-ray features of OA and (2) 6 control subjects (matched to cases for age, sex and body mass index in a 1:2 ratio) who do not have clinical features of OA.

Participants will undergo an initial (baseline) MR examination, followed by repeat MR examinations at approximately 1 month and 1 year following the baseline examination.

This will allow the investigators to explore the possibility of mechanical joint-loading and exercise to differentiate early stage OA from healthy subjects and assess both the reliability of the MR measurements and the expected progression in the MR measurements in OA subjects in the absence of any disease-modifying intervention.

Condition or Disease Intervention/Treatment Phase
  • Device: Magnetic resonance imaging (MRI)

Study Design

Study Type:
Observational
Actual Enrollment :
18 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Functional Exercise Response on osteoArthritis Relaxation Imaging
Actual Study Start Date :
Nov 21, 2019
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Healthy volunteers

Device: Magnetic resonance imaging (MRI)
Participants will undergo an initial (baseline) MR examination, followed by repeat MR examinations at approximately 1 month and 1 year following the baseline examination.

Osteoarthritis patients

Device: Magnetic resonance imaging (MRI)
Participants will undergo an initial (baseline) MR examination, followed by repeat MR examinations at approximately 1 month and 1 year following the baseline examination.

Outcome Measures

Primary Outcome Measures

  1. Establish effect sizes for MR parameters in OA patients compared to healthy volunteers. [1 year]

Secondary Outcome Measures

  1. Establish effect sizes for MR parameters in subjects with OA at 1 year compared to baseline. [1 year]

  2. Establish reliability of the MR protocol and analysis techniques. [1 month - 1 year]

    Test-Retest Reliability

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Group 1 Inclusion Criteria:
  • Meets ACR criteria for OA Kellgren-Lawrence grade 2-3 on knee radiograph

  • Neutral alignment

  • Single symptomatic joint

  • Aged 40-60 years old

  • Ambulatory and in good general health

  • Knee able to fit inside in-vivo knee coil (approx. 18 cm diameter)

Group 2 Inclusion Criteria:
  • No current symptoms of knee pain or stiffness or other clinical features of OA

  • Aged 40-60 years old

  • Written consent to participate in the study

  • Ambulatory and in good general health

  • Knee able to fit inside in-vivo knee coil (approx. 18 cm diameter)

Exclusion Criteria for both groups:
  • History of ipsilateral lower limb fracture

  • History of ipsilateral lower limb surgery (including arthroscopy)

  • Metabolic bone disease

  • Inflammatory arthritis

  • Haematological malignancy

  • Paget's disease

  • Bone metastases

  • Contraindication to MR imaging (e.g. pacemaker, severe claustrophobia)

  • No pregnant patients will be included

  • Unable to consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Addenbrooke's Hospital Cambridge Cambridgeshire United Kingdom CB2 0QQ

Sponsors and Collaborators

  • Cambridge University Hospitals NHS Foundation Trust

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Professor Fiona J Gilbert, Head of Department - Radiology, Cambridge University Hospitals NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT03657303
Other Study ID Numbers:
  • A094874
First Posted:
Sep 5, 2018
Last Update Posted:
Jul 20, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Professor Fiona J Gilbert, Head of Department - Radiology, Cambridge University Hospitals NHS Foundation Trust
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 20, 2022