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RecruitingNCT07795008Updated Aug 31, 2026

Evaluation of Sport Injuries of Knee by MRI

An observational study in Sports-related Knee Injuries, sponsored by Sohag University. Recruiting at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2026-08-31.

Sponsored by Sohag University · Observational

From the registry’s dates

  • Started Jul 2026; still recruiting 3 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Sex
All
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Study summary

This study will evaluate how well magnetic resonance imaging (MRI) can detect and characterize sports-related knee injuries. The study will include patients with sports-related knee injuries who undergo MRI examination. The MRI findings will be assessed for injuries involving the ligaments, menisci, cartilage, tendons, muscles, and bones, as well as other associated abnormalities. The study will also examine how MRI findings compare with the clinical diagnosis. The goal is to better understand the patterns and characteristics of sports-related knee injuries and the usefulness of MRI in their diagnosis and management.

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Conditions studied

  • Sports-related Knee Injuries

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In context

Knee Injuries

267 studies on the registry are indexed under Knee Injuries; 59 are open to participants now.

This study's planned enrollment of 50 is below the median of 82 across 79 observational studies indexed under Knee Injuries.

Browse Knee Injuries studies →

Lead sponsor

Sohag University is the lead sponsor of 1,230 studies on the registry; 636 are open to participants now.

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

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients of any age and either sex presenting with sports-related knee injuries and undergoing MRI examination at the Diagnostic and Interventional Radiology Department, Sohag University Hospitals. The study will include 50 participants who meet the eligibility criteria.

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

  • Patients of any age with sports-related knee injuries.

    • Both males and females.
    • Patients willing to participate in the study and provide .

Exclusion criteria

  • to MRI.

    • Non-sports-related knee injuries.
    • Previous knee surgery.
    • Osteoarthritic changes of the knee.
    • Patients who refuse to participate.
Terms in these criteria, in plain language(2)

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.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patients with Sports-Related Knee Injuries

    Patients of any age and either sex presenting with sports-related knee injuries who meet the study eligibility criteria and undergo MRI of the knee. Patients with MRI contraindications, non-sports-related knee injuries, previous knee surgery, osteoarthritic changes, or those who decline participation will be excluded.

    Diagnostic Test: Magnetic Resonance Imaging (MRI) of the Knee

Interventions

  • Diagnostic testMagnetic Resonance Imaging (MRI) of the Knee

    Participants will undergo magnetic resonance imaging (MRI) of the knee using a 1.5-Tesla MRI scanner. The MRI examination will include sagittal T1-weighted, sagittal T2-weighted, sagittal proton-density (PD) fat-suppressed, coronal T1-weighted, coronal PD fat-suppressed, axial T2-weighted, and axial PD fat-suppressed sequences. STIR imaging will be performed when indicated. MRI findings will be assessed for ligamentous, meniscal, cartilage, tendon, muscle, and bone injuries, as well as associated abnormalities such as joint effusion and Baker cyst.

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What researchers measure

Primary outcomes

  1. Diagnostic accuracy of MRI in detecting sports-related knee injuries

    MRI findings will be assessed for the detection and characterization of ligamentous, meniscal, cartilage, tendon, muscle, and bone injuries in patients with sports-related knee injuries. Diagnostic performance will be evaluated using sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy.

    Time frame: At the time of MRI examination (single assessment during the study visit).

Secondary outcomes

  1. Distribution and characterization of sports-related knee injuries on MRI

    The study will evaluate the patterns and types of MRI-detected knee injuries, including ACL, PCL, collateral ligament, meniscal, cartilage, tendon, muscle, and bone injuries, as well as associated findings such as joint effusion and Baker cyst.

    Time frame: At the time of MRI examination (single assessment during the study visit).

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Study locations

1 of 1 sites recruiting
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References and documents

Publications

  • Ho CP, Marks PH, Steadman JR. MR imaging of knee anterior cruciate ligament and associated injuries in skiers. Magn Reson Imaging Clin N Am. 1999 Feb;7(1):117-30. PubMed 10067227 ↗
  • Fritz B, Fritz J. MR Imaging of Acute Knee Injuries: Systematic Evaluation and Reporting. Radiol Clin North Am. 2023 Mar;61(2):261-280. doi: 10.1016/j.rcl.2022.10.005. PubMed 36739145 ↗

Individual participant data

Plan to share: No

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2026 (actual). Primary completion is estimated for Jun 2027, 11 months after the start.

Of 30 observational studies under Knee Injuries, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 56. This study's planned 11 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 25, 2026
First posted
Aug 31, 2026
StartActual
Jul 13, 2026
Primary completionEst.
Jun 2027
CompletionEst.
Jul 2027
Last update
Aug 31, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07795008
Lead sponsor
Sohag University
Responsible party
Rania Gamal Mahmoud (Resident in Diagnostic and Interventional Radiology Department, Sohag University) — Principal investigator
First posted
Aug 31, 2026
Start date
Jul 13, 2026
Primary completion
Jun 2027 (estimated)
Completion
Jul 2027 (estimated)
Last update
Aug 31, 2026

Study contacts

Rania Gamal Mahmoud
Contact
01126738258rr@gmail.com
+201126738258

Oversight

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

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