- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04979117
Superb Microvascular Imaging Ultrasonography of Plantar Fasciitis (SMI)
Diagnostic Performance of Superb Microvascular Imaging Ultrasonography in Plantar Fasciitis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Plantar fasciitis (PF) is a painful condition of the inferior and medial heel. Symptoms worsens with the first steps in the morning or after prolonged sitting and long periods of standing.
The diagnosis of PF is made according to the typical anamnesis and physical examination, based on the emerge of local point tenderness over the heel and proximal fascia due to the pressure applied by the physician. Heel pain exacerbates by the first steps in the morning or after rest and with prolonged standing. Unless there is an inflammatory disease such as spondyloarthropathy, there is no laboratory finding indicating plantar fasciitis. Imaging methods are very useful for making an accurate diagnosis. Because the main problem is in the soft tissue, plain radiography has limited diagnostic value, but can be helpful in identifying calcaneal stress fractures.
Magnetic resonance imaging (MRI) is very successful in showing the inflammatory process of soft tissue. However, it does not seem possible to use MRI scans routinely because of the cost and time it requires.
PF can be evaluated with ultrasonography with the advantages of being non-invasive, relatively inexpensive, easy to access and apply, and is increasingly used in clinical practice. Color Doppler evaluation is a very valuable part of musculoskeletal sonographic examination and facilitates the clinician's decision as an inflammation marker. Power Doppler US is quite sensitive to tissue or probe movement, especially at low pulsed repetition frequency (PRF). Flash artifacts may be observed. However, Doppler USG has limited sensitivity at low flows and small vessel structures.
Superb microvascular imaging (SMI) (Toshiba Medical Systems, Tokyo, Japan) is a new mode of vascular imaging that provides visualization of activity in microvascular structures or in structures that have low flow rate.
To the best of our knowledge, there are no studies comparing the diagnostic performance of the SMI modality in plantar fasciitis with color Doppler and gray scale US. Therefore, a prospective study will be conducted to evaluate the diagnostic performance of SMI, gray scale US, color Doppler US and Power Doppler US. The null hypothesis that there is no difference between Doppler US and SMI methods in the detection of increased inflammatory activity in plantar fasciitis patients.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Ender Salbas, MD
- Phone Number: +905556698639
- Email: drendersalbas@gmail.com
Study Contact Backup
- Name: Ender Salbas, MD
- Phone Number: +905556698639
- Email: drender@yandex.com
Study Locations
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Niğde, Turkey, 51700
- Nigde Omer Halisdemir University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
- Patients who diagnosed as Plantar Fasciitis as the first group
- Healthy participants as the second group
Description
For the first group:
Inclusion Criteria:
- Patients who diagnosed as Plantar Fasciitis
- Age between 18-45
Exclusion Criteria:
- History of foot trauma or surgery
- Diabetes mellitus
- Pregnancy,
- Rheumatological diseases
For the second group:
Inclusion Criteria:
- asymptomatic foot,
- no previous trauma or surgery on foot,
- no history of systemic inflammatory disorders.
Exclusion Criteria:
- History of foot trauma or surgery
- Diabetes mellitus
- Pregnancy,
- Rheumatological diseases
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Participants with plantar fasciitis
Participants with the diagnose of plantar fasciitis; typical anamnesis (exacerbating pain by the first steps in the morning or after rest and with prolonged standing). The emerge of local point tenderness over the heel and proximal fascia due to the pressure applied by the physician. Thickening of the plantar fascia greater than 4 mm in ultrasonographic evaluation. measurement |
to determine whether there is a diagnostic value of SMI in Plantar Fasciitis and whether there is a superiority when compared Power Doppler and Color Doppler modalities.
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Volunteers who has not foot complaints.
Volunteers who were not diagnosed with Plantar Fasciitis and without foot or heel pain when taking the first steps in the morning, with plantar fascia thickness less than 4 mm, painless, symptom-free and which had no additional rheumatic disease.
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to determine whether there is a diagnostic value of SMI in Plantar Fasciitis and whether there is a superiority when compared Power Doppler and Color Doppler modalities.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Visual Analog Scale (VAS) Pain Score
Time Frame: Each participant will be assessed only one time at the admission time to the outpatient clinic
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The patient will be asked to indicate his/her perceived pain intensity (most commonly) along a 100 mm horizontal line.
This rating is then measured from the left edge gives the VAS score.
A higher score indicates greater pain intensity and lower scores indicates less pain intensity.
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Each participant will be assessed only one time at the admission time to the outpatient clinic
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Heel Tenderness Index (HTI)
Time Frame: Each participant will be assessed only one time at the admission time to the outpatient clinic
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Heel tenderness index (HTI) will be assessed by physician; based on assessing pain on palpation (0=no pain, 1=painful, 2=painful and winces, 3=painful, winces and withdraws).
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Each participant will be assessed only one time at the admission time to the outpatient clinic
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Foot Function Index (FFI)
Time Frame: Each participant will be assessed only one time at the admission time to the outpatient clinic
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This index aims to measure the impact of foot pathology on function in terms of pain, disability and activity restriction.
The FFI is a self-administered index consisting of 23 items divided into 3 sub-scales.
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Each participant will be assessed only one time at the admission time to the outpatient clinic
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Ultrasonographic Evaluation; Superb Microvascular Imaging, GrayScale Imaging, Color Doppler Imaging, Power Doppler Imaging
Time Frame: Each participant will be assessed only one time at the admission time to the outpatient clinic
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Vascular blood flow images from median nerve (enterrapted in carpal tunnel) obtained with Power Doppler and Superb microvascular imaging.
[ Time Frame: Each participant will be assessed only one time at the admission time to the outpatient clinic ] Four-stage classify will be use for grading these images; Grade 0: No vascularity in MN, Grade 1: One or two focal color-encoded spots in MN, Grade 2: One linear color-encoded line or more than two focal color-encoded spots in MN, Grade 3: More than one linear color-encoded line in MN
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Each participant will be assessed only one time at the admission time to the outpatient clinic
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Ender Salbas, MD, Omer Halisdemir University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ES01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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