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Comparison of Ultrasonographic and Clinical Features of Different Energy Levels Extracorporeal Shock Wave Therapy in Plantar Fasciitis

B

Baskent University Ankara Hospital

Status

Unknown

Conditions

Extracorporeal Shock Wave Therapy

Treatments

Device: Extracorporeal Shock Wave Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT04989530
E-94603339-604.01.02-46403

Details and patient eligibility

About

Plantar fasciitis is the most common cause of heel pain in adults. It received FDA approval in 2000 for ESWT in the treatment of plantar fasciitis in adults whose pain did not resolve with conservative treatment.

ESWT energy levels are categorized as high, medium and low. It is not yet clear which energy level is most effective in the clinical recovery and pain relief of plantar fasciitis after ESWT treatment. Although there are studies in the literature evaluating the effect of different energy densities in the treatment of plantar fasciitis with ESWT, there are very few studies comparing different treatment doses of ESWT.

The aim of this study was to evaluate and compare the therapeutic effects of low, medium and high energy ESWT in patients with plantar fasciitis, and also to examine the correlation between plantar fascia thickness changes ultrasonographically and clinical outcomes.

Enrollment

78 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

presence of heel pain, tenderness at the insertion site of the plantar fascia on the anteromedial aspect of the calcaneal tubercle elicited by palpation, and unresponsiveness to medical treatment.

Exclusion criteria

history of inflammatory rheumatic disease, trauma of the foot or foot surgery, local dermatological lesion or infection, impaired peripheral circulation, a neurological disorder such as radiculopathy and neuropathy, patients with sequelae of lower extremity fracture, a congenital or acquired deformity, malignancy, cardiac pacemaker, metal implant at the application site, pregnancy, anticoagulant use for coagulopathy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

78 participants in 3 patient groups

Low energy level of ESWT
Active Comparator group
Treatment:
Device: Extracorporeal Shock Wave Therapy
medium energy level of ESWT
Active Comparator group
Treatment:
Device: Extracorporeal Shock Wave Therapy
high energy level of ESWT
Active Comparator group
Treatment:
Device: Extracorporeal Shock Wave Therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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