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The Effect of the Dry Needle on heel spur in Compared to Extracorporeal Shock Wave Therapy (ESWT)

Phase 1
Conditions
Plantar Fasciitis.
Plantar fascial fibromatosis
Registration Number
IRCT201610014104N6
Lead Sponsor
Physical Medicine Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
72
Inclusion Criteria

Inclusion Criteria: All patient with Plantar Fasciitis? without responses to usual medical ? treatment after one moon .

Exclusion Criteria

inflammatory disease such as (RA)? history of trauma ? history of local injection or PT in tree moons ago ? heel pain associated with Achill bursitis ? active S1 radiculopathy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Daily pain intensity. Timepoint: Before treatment and 4 and 8 weeks after treatment. Method of measurement: Visual Analog Scale.
Secondary Outcome Measures
NameTimeMethod
The rate of recovery. Timepoint: Before treatment and 4 and 8 weeks after treatment. Method of measurement: Foot Function Index - Visual Analog Scale.
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