Comparative Effectiveness of the Customized poly-propylene Semi-rigid Insole and Prefabricated SiliconeHeel Pad in Pain Reduction and Functional Improvement of Patients with Plantar Fasciitis

Phase 2

Recruiting

• Conditions: plantar fasciitis.; Plantar fascial fibromatosis; M72.2

• Registration Number: IRCT20191129045542N2
• Lead Sponsor: Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 54

Inclusion Criteria

Sharp, shooting or localized pain in the sole of the foot for at least one month- 18 year-old patients or older.- Tenderness along the posteromedail aspect of the longitudinal arch or medial calcaneal tubercle.- Start-up pain in the morning with ambulation.- Decrease pain after walking

Exclusion Criteria

- Any lower extremity injuries including foot and ankle within 6 months.- Stress fracture- Receiving plantar steroid injection within 3 months.- Use of nonsteroidal anti-inflammatory medications within the previous one week.- Use of custom foot orthotics previously.- Other painful foot condition such as bunion, corn, or ingrown toe nail.- Any other lower extremity neuromuscular conditions such as active radiculopathy- Non-ambulatory, non-communicative.-Unable to complete the interview .- Spasticity due to a neurologic disorder.-Previous foot surgery.- Congenital defects of the lower extremity..- Diabetic mellitus

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain reduction and foot functional improvement. Timepoint: Before, 3 and 12 weeks after treatment. Method of measurement: Visual Analog Scale, Foot Function Index.