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Clinical Trials/NCT06023836
NCT06023836
Completed
Not Applicable

Myofascial Pain Syndrome in Plantar Fasciitis; Comparison of Dry Needling and Extracorporeal Shockwave Therapy (ESWT) Effects on Pain and Function

Istanbul Training and Research Hospital1 site in 1 country66 target enrollmentMay 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Plantar Fascitis
Sponsor
Istanbul Training and Research Hospital
Enrollment
66
Locations
1
Primary Endpoint
Function was evaluated with (Foot Functional Index) FFI score.
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Patients with plantar fasciitis between the ages of 25-65 years who presented to the Physical Medicine and Rehabilitation clinic with the complaint of heel pain and met the inclusion and exclusion criteria will be included in the study. Demographic data (age, gender, body mass index, symptom duration) will be recorded at the beginning of the study. Then, Foot Functional Index (FFI) and Visual Analog Scale (VAS) scales will be recorded. Participants will be randomly divided into two groups. Group 1 will receive dry needling and Group 2 will receive extracorporeal shock wave therapy (ESWT). Patients in the 1st group will undergo 3 sessions of dry needling with Seirin branded 0.6*50 mm acupuncture needles at one week intervals for the trigger point detected by manual palpation in the medial gastrocnemius, lateral gastrocnemius, soleus, flexor digitorum brevis, quadratus plantae, abductor hallucis brevis muscles. Patients in the 2nd group, Patients in this group received three sessions of ESWT (MASTERPLUS MP 200 ENERGY 2 trademarked ESWT device) at an energy density of 2 bars and a frequency of 2,000 shocks/min at 12 Hz for three weeks, each session once a week. Each of the five most sensitive and painful points was given 400 pulses in the supine position

Registry
clinicaltrials.gov
Start Date
May 1, 2023
End Date
September 8, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul Training and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Burak Tayyip Dede

Medical Doctor

Istanbul Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients aged 25-65 years with heel pain for more than 6 weeks
  • tenderness on palpation in the medial calcaneal region
  • aggravation of symptoms while standing and in the first hours of the morning
  • who agreed not to receive anti-inflammatory treatment during the study period
  • fascia thickness \>4mm measured by ultrasound.

Exclusion Criteria

  • Patients diagnosed with rheumatologic diseases
  • Those diagnosed with Diabetes Mellitus (DM), those with chronic liver and kidney failure
  • Anti-inflammatory-analgesic treatment within the last 1 month
  • Diagnosed with inflammatory rheumatic disease
  • Those with a history of foot surgery
  • Those with mid or hindfoot deformity
  • Previous history of central or peripheral nerve damage, lower extremity neuropathy
  • Those diagnosed with Diabetes Mellitus
  • Those with cognitive impairment
  • Unassisted mobilization

Outcomes

Primary Outcomes

Function was evaluated with (Foot Functional Index) FFI score.

Time Frame: 5 months

Comparison of the effects of ESWT and dry needling on function in the management of plantar fasciitis

Pain was evaluated with a Visual analog scale (VAS) score.

Time Frame: 5 months

VAS score ranges from 0 to 10. Comparison of the effects of ESWT and dry needling on pain in the management of plantar fasciitis

Study Sites (1)

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