ClinicalTrials.gg
Not yet recruitingNCT07827443Updated Sep 18, 2026

mFFE MRI Versus CT for Cortical Bone Evaluation in Knee Osteoarthritis

An observational study in Osteoarthritis, Knee and Bone Diseases, sponsored by Assiut University. Not yet recruiting. Open to participants aged 40 Years and older. Per ClinicalTrials.gov, last updated 2026-09-18.

Sponsored by Assiut University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
80
Ages
40 Years and older
Sex
All
01

Study summary

This cross-sectional study aims to evaluate the accuracy of multi-echo fast field echo (mFFE) MRI in depicting cortical bone changes in knee osteoarthritis compared with CT.

Read the detailed description

Knee osteoarthritis involves microstructural alterations in subchondral and cortical bone. Conventional MRI has limitations in visualizing cortical bone due to short T2 relaxation times. Multi-echo fast field echo (mFFE) sequences can produce CT-like images of cortical bone without ionizing radiation.

This observational study will include patients aged 40 years or older with clinically suspected or confirmed knee osteoarthritis. All participants will undergo both mFFE MRI and CT of the knee. The accuracy of mFFE MRI in detecting cortical bone degenerative changes will be compared with CT as the reference standard.

02

Conditions studied

  • Osteoarthritis, Knee
  • Bone Diseases

Keywords

  • mFFE MRI
  • Knee osteoarthritis
  • Cortical bone
  • CT-like MRI
  • Assiut
03

In context

Osteoarthritis, Knee

3,292 studies on the registry are indexed under Osteoarthritis, Knee; 623 are open to participants now.

This study's planned enrollment of 80 is below the median of 100 across 486 observational studies indexed under Osteoarthritis, Knee.

Browse Osteoarthritis, Knee studies →

Lead sponsor

Assiut University is the lead sponsor of 5,078 studies on the registry; 2,178 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients aged 40 years or older with clinically suspected or confirmed knee osteoarthritis attending the Diagnostic and Interventional Radiology Department at Assiut University Hospital.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • - Age 40 years or older
  • Clinically suspected or confirmed knee osteoarthritis
  • Able and willing to provide

Exclusion criteria

Exclusion Criteria:

  • - Implanted electronic devices (pacemakers, ICDs, neurostimulators, cochlear implants)
  • Metallic foreign bodies in the eyes or orbits
  • Ferromagnetic cerebral aneurysm clips
  • Implantable infusion pumps
  • Pregnancy
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
80 participants (estimated)
Patient registry
No

Groups and cohorts

  • Single cohort: Patients with knee osteoarthritis

    Patients aged 40 years or older with knee osteoarthritis who will undergo both multi-echo fast field echo (mFFE) MRI and CT of the knee for comparison of cortical bone evaluation.

06

What researchers measure

Primary outcomes

  1. Diagnostic accuracy of mFFE MRI for cortical bone changes

    Overall diagnostic accuracy percentage of multi-echo fast field echo MRI in detecting cortical bone degenerative changes in knee osteoarthritis, using CT as the reference standard

    Time frame: Baseline

Secondary outcomes

  1. Sensitivity of mFFE MRI for cortical bone changes

    Sensitivity percentage of multi-echo fast field echo MRI in detecting cortical bone degenerative changes in knee osteoarthritis, using CT as the reference standard

    Time frame: Baseline

  2. Specificity of mFFE MRI for cortical bone changes

    Specificity percentage of multi-echo fast field echo MRI in detecting cortical bone degenerative changes in knee osteoarthritis, using CT as the reference standard

    Time frame: Baseline

  3. Detection of subchondral sclerosis

    Number of cases in which mFFE MRI correctly identifies subchondral sclerosis compared with CT

    Time frame: Baseline

  4. Detection of osteophytes

    Number of cases in which mFFE MRI correctly identifies osteophytes compared with CT

    Time frame: Baseline

  5. Detection of joint space narrowing

    Number of cases in which mFFE MRI correctly identifies joint space narrowing compared with CT

    Time frame: Baseline

  6. Image quality score

    Mean subjective image quality score of mFFE MRI for cortical bone visualization on a predefined scale from 1 to 5, with higher scores indicating better image quality

    Time frame: Baseline

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07827443
Lead sponsor
Assiut University
Responsible party
Fatima Mahmoud Hammad Eltony (Resident Physician, Assiut University) — Principal investigator
First posted
Sep 18, 2026
Start date
Sep 15, 2026 (estimated)
Primary completion
Sep 20, 2027 (estimated)
Completion
Feb 20, 2028 (estimated)
Last update
Sep 18, 2026

Study contacts

Fatima M Eltony, Resident
Contact
fatima.18313255@med.aun.edu.eg
+20 10 15712606
Ehab M Mohammed, prof
study chair · Diagnostic and interventional radiology Department, Assiut University Hospitals

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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