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Active, not recruitingNCT07802795Hip MRIUpdated Sep 3, 2026

Role of Magnetic Resonance Imaging in Assessment of Patients With Hip Pain

An observational study in Hip Pain &Disorders, sponsored by Sohag University. Active, not recruiting at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2026-09-03.

Primary conditionnone(registry's first term: Disease)No conditionIs this wrong?Disease describes something many studies share rather than a condition a study is about. The study names no condition we can place it under, so it is not compared with other studies by condition.

Sponsored by Sohag University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Sex
All
01

Study summary

To evaluate the role of Magnetic Resonance Imaging in the assessment and diagnosis of patients presenting with hip pain.

Read the detailed description

The hip joint is a deep ball-and-socket synovial joint formed by the articulation between the femoral head and the acetabulum, supported by the labrum, ligaments, and surrounding musculature. This structural complexity makes clinical evaluation alone insufficient for identifying the underlying pathology. Magnetic Resonance Imaging (MRI) has emerged as a key imaging modality for comprehensive assessment of both normal anatomy and pathological conditions affecting the hip joint

02

Conditions studied

  • Hip Pain &Disorders

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Keywords

  • Hip pain
03

In context

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.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

the study population will consist of patients presenting with hip pain who are referred for MRI evaluation of the hip. patients of all age groups and both sexes will be eligible for inclusion. the study will assess MRI findings and characterize the underlying abnormalities associated with hip pain, including osseous, articular, and periarticular soft tissue abnormalities. patients with MRI contraindications or technically inadequate examination will be excluded.

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 and sex.
  • Patients complaining of hip pain.
  • Patients fit for MRI examination.

Exclusion criteria

Exclusion Criteria:

  • Patients with to MRI (e.g. pacemakers, cochlear implants).
  • Claustrophobic patients who cannot tolerate MRI examination.
  • Patients with renal impairment contraindicating contrast administration (if contrast is needed).
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.

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 hip pain

    no intervention, participants will undergo MRI examination for assessment of hip pain and identification of underlying hip abnormalities

06

What researchers measure

Primary outcomes

  1. Diagnostic yield of MRI in identifying the underlying cause of hip pain.

    Proportion of patients in whom MRI identifies a specific structural or pathological abnormality that may explain the presenting hip pain, including labral tears, cartilage abnormalities, femoroacetabular impingement, avascular necrosis, stress/insufficiency fractures, bone marrow edema, osteoarthritis, joint effusion/synovitis, tendinopathy, bursitis, and other periarticular soft-tissue abnormalities.

    Time frame: At the time of MRI examination

Secondary outcomes

  1. Distribution of MRI-detected pathologies in patients presenting with hip pain.

    Frequency and type of abnormalities detected by MRI, categorized into osseous, articular, labral, synovial, muscular, tendinous, bursal, and other soft-tissue abnormalities.

    Time frame: at the time of MRI examination

  2. Correlation between MRI findings and clinical presentation.

    Assessment of the association between MRI abnormalities and clinical characteristics, including age, sex, laterality, duration and characteristics of hip pain, and relevant clinical diagnosis.

    Time frame: At the time of MRI examination.

07

Study locations

1 site
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References and documents

Individual participant data

Plan to share: No — There are no plans to share individual participant data (IPD) due to privacy and confidentiality considerations.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Dec 2025 (actual). Primary completion is estimated for Jan 2027, 12 months after the start.

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

Registered
Aug 9, 2026
First posted
Sep 3, 2026
StartActual
Dec 10, 2025
Primary completionEst.
Jan 1, 2027
CompletionEst.
Feb 1, 2027
Last update
Sep 3, 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 Sep 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07802795
Lead sponsor
Sohag University
Responsible party
Omnia Ashraf Ahmed (Ameen) (Resident, Sohag University) — Principal investigator
First posted
Sep 3, 2026
Start date
Dec 10, 2025
Primary completion
Jan 1, 2027 (estimated)
Completion
Feb 1, 2027 (estimated)
Last update
Sep 3, 2026

Study contacts

Mohamad Hasan Alam-Eldeen, MD
principal investigator

Oversight

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

Not currently enrolling

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

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Discussion

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