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Comparison between the radial shockwave therapy at plantar fascia and combined the radial shockwave therapy at plantar fascia and gastrocnemius in chronic plantar fasciitis treatment: A Prospective, Randomized, Controlled Trial

Comparison between the radial shockwave therapy at plantar fascia and combined the radial shockwave therapy at plantar fascia and gastrocnemius in chronic plantar fasciitis treatment: A Prospective, Randomized, Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250714008
Enrollment
84
Registered
2025-07-14
Start date
2016-06-09
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

A plantar fasciitis A plantar fasciitis radial shockwave therapy

Interventions

Patients received conventional physiotherapy plus radial shockwave therapy at the plantar fascia and gastrocnemius muscle. ,Patients received conventional physiotherapy plus radial shockwave therapy a
RSWT group,Control group

Sponsors

Faculty of Medicine, Chiang Mai University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis of plantar fasciitis, with clinical start up pain of heel, tenderness at medial tubercle of calcaneal tuberosity and plantar fascia thickness greater than 4 mm, as assessed using ultrasonography (Sonosite, Bothell, WA 98021 USA) 2. Age more than 20 years old 3. Painful symptoms for three months or more 4. Ability to come to the hospital for evaluation and treatment

Exclusion criteria

Exclusion criteria: 1. using a heart pacemaker or anticoagulant medication coagulopathy and other musculoskeletal conditions of any etiology with clinical manifestations in the lower limbs and spine 2. central or peripheral neuropathy 3. systemic inflammatory disease, associated metabolic and endocrine diseases and psychiatric disorders 4. previous surgery of the foot 5. previous fracture of ankle and foot 6. previous corticosteroid injection at plantar fascia within 3 months

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS) for morning pain, pain during walking pretreatment, first, second, third, fourth session after treatment, 3, 6 and 12 months (follow-up). VAS pain scale,frequency of pain pretreatment, first, second, third, fourth session after treatment, 3, 6 and 12 months (follow-up). Times per week

Secondary

MeasureTime frame
range of motion (ROM) of ankle, ankle dorsiflexion using an digital goniometer device pretreatment and 12 months (follow-up). degree

Countries

Thailand

Contacts

Public ContactTanawat Vaseenon

Faculty of Medicine, Chiang Mai University

tvaseenon@yahoo.com0835150933

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026