Is Ultrasonography Comparable to MRI for the Detection of Morton Neuroma of the Foot?
NCT ID: NCT00284414
Last Updated: 2021-07-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
NA
INTERVENTIONAL
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
In case of surgery, the pathology report will be compared with the ultrasonographic or MRI findings.
Which is the most reliable and specific: ultrasonography or MRI?
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Correlation Between Fasicitis Plantaris and Hallux Rigidus
NCT00285116
Comparison of the Effects of Morton's Neuroma on Foot Pressure Distribution and Gait Parameters in Pes Planus and Pes Cavus Patients
NCT05012488
Morton's Neuroma: Manipulation Versus Steroid Injection
NCT02304094
Morton's Neuroma: Manipulation Versus Steroid Injection
NCT05707572
Weight-Bearing Tomosynthesis In Evaluation of Foot/AnkIe
NCT02432170
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Ultrasonography or MRI
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
20 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Ghent
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Rene Verdonk, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Ghent
Related Links
Access external resources that provide additional context or updates about the study.
Website University Hospital Ghent
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2004/199
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.