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The effect of dry needling on pain and Range of Motion of ankle joint and thickness of plantar fascia in patient with plantar fasciitis

Phase 2
Conditions
Plantar fasciitis.
Plantar fasciitis
Registration Number
IRCT2017080525732N22
Lead Sponsor
Deputy of Research and Technology, Semnan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Patients with PFs in aged 40 to 60 years; having trigger point in gastro or soleus muscles or both of them; thickness plantar fascia more than 4 mm; foot pain in first steps in the morning and at least six months has passed since the onset of pain; the pain level in visual analog scale is at least four; non-athlete persons; plantar flexion or dorsi flexion is less than normal range.
Exclusion criteria: Diabetes; hypersensitivity to needle; fear of needle; pregnancy; infection; peripheral neuropathy; hemophilia or coagulation problems; history of plantar fascia surgery; history of injection in the last three months.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Plantar Fascia Thickness. Timepoint: Before and after using a dry needle. Method of measurement: Ultrasonography.
Secondary Outcome Measures
NameTimeMethod
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