Magnetic Resonance Imaging to Assess Changes in Meniscus Vascularity (MOVE)

The Leeds Teaching Hospitals NHS Trust

Status: Unknown

Conditions: Meniscus Tears

Treatments: Other: Will undergo a single MRI assessment with intravenous dye; Other: pre and post surgery MRI scan

Study type: Interventional

Funder types: Other

Identifiers

NCT02363140

OR11/9770

Details and patient eligibility

About

The menisci in the knee joint are important for normal functioning of the knee. Meniscus tears are amongst the commonest of injuries to the knee. The pattern and blood supply of the meniscus tears determines the treatment plan and outcome. The surgeon identifies the blood supply to the meniscus tear area during the arthroscopy(key hole operation) and decides the treatment option ie repair versus partial meniscectomy.

This study aims to identify any changes that occur in the meniscus blood supply. The following are the main aims of the 'MOVE'study-

1. Use of non-invasive methods ie MRImaging to assess meniscus vascularity to preoperatively plan treatment and advice patient on recovery.
2. The study would assess changes in meniscus blood supply depending on age of the patient.
3. The study aims to assess the alteration in meniscus blood supply following an arthroscopic(key hole) meniscal repair operation.

Enrollment: 48 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Inclusion criteria for Group I,II

1. Patients should be aged 18-20 years or 35-45years
2. Asymptomatic knee for past 6 months.
3. Painless flexion-extension movements at knee joint.

Inclusion criteria for Group III

1. Patients should be aged 75 or older
2. Knee X-ray showing no more than Kellgren-Lawrence grade II osteoarthrtis
3. No clinical suspicion of meniscus tear
4. Painless flexion-extension movements at knee joint.

Inclusion criteria for Group IV

1. Patients should have presented with clinical signs to suggest meniscus tear indicating potential need for surgical meniscus repair.

Exclusion criteria

1. Proven Polyarthritis / Polyarthralgia secondary to Rheumatoid arthritis, Gout, Lupus, Ankylosing Spondylosis, Psoriatic arthritis
2. Any previous surgical procedure(open or arthroscopic) involving the knee joint.(baring the current meniscus repair in Group IV participants)
3. Patients unable to give informed consent.
4. Patients with contraindication for MR Imaging - Metal implants, prosthetic heart valves, pacemakers, metal foreign bodies, VP shunts, pregnancy, cochlear implant, metal clips in the brain, Patients with static tremor i.e. Parkinson's disease.
5. Patients with contraindications for contrast agent - Renal impairment, Previous allergic reaction.

Trial design

48 participants in 4 patient groups

Group One patients in age group 18--20 years,

No Intervention group

Description:

1. Patients should be aged 18--20 years or 35--45years 2. Asymptomatic knee for past 6 months. 3. Painless flexion-extension movements at knee joint.

Group Two patients in age group 35-45 years,

Active Comparator group

Description:

1. Patients should be aged 18--20 years or 35--45years 2. Asymptomatic knee for past 6 months. 3. Painless flexion-extension movements at knee joint.

Treatment:

Other: Will undergo a single MRI assessment with intravenous dye

Group Three Patients aged 75

Active Comparator group

Description:

1. Patients should be aged 75 or older 2. Knee X-ray showing no more than Kellgren-Lawrence grade II osteoarthrtis 3. No clinical suspicion of meniscus tear 4. Painless flexion-extension movements at knee joint.

Treatment:

Other: Will undergo a single MRI assessment with intravenous dye

Group Four, any age due to undergo a surgical meniscus repair

Active Comparator group

Description:

1. Patients should have presented with clinical signs to suggest meniscus tear indicating potential need for surgical meniscus repair

Treatment:

Other: pre and post surgery MRI scan