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A clinical trial to compare the effect of three physiotherapeutic treatments - High Intensity LASER therapy, Extracoporeal Shockwave therapy and Ultrasound therapy in patients diagnosed with plantar fasciitis

Effect of High Intensity LASER therapy, Extracorporeal Shockwave therapy and Ultrasound therapy in patients with Plantar Fasciitis: A Randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015493
Enrollment
120
Registered
2018-08-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: M796- Pain in limb, hand, foot, fingersand toes Health Condition 2: null- Plantar Fasciitis

Interventions

Intervention1: High Intensity LASER therapy: Dosage: 10 W, 450J/cm2, 3 sessions / week for 2 weeks Intervention2: Extracorporeal Shockwave therapy: Dosage: 2 bar, 2000shots, 5 Hz, 2 sessions / week fo

Sponsors

R Ravindran
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age group 18 to 65 years 2. Persons with Plantar fasciitis with tenderness on the medial tubercle of calcaneus, maximum pain in the heel during the first few steps in the morning or after prolonged inactivity and VAS more than or equal to 3 3. Both male and female patients will be recuited

Exclusion criteria

Exclusion criteria: Patients with the following criteria will be excluded from the study 1. Heel pain due to any other problem except plantar fasciitis 2. Previous history of local surgery of foot 3. Any fractures involving foot bones 4. Posterior heel pain due to Achilles tendon / bursitis 5. Metal implants, impaired sensations and stiffness in ankle and foot. 6. Neurological and vascular disease. 7. Systemic inflammatory disease 8. Uncontrolled Diabetes mellitus 9. Patients who had received a corticosteroid injection or invasive therapy for plantar fasciitis within the previous 6 months or physiotherapy within the previous 3 months 10. With associated lower limb Radiculopathy

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale Pain Perception threshold Timepoint: Pre-Treatment and Post-Treatment (After 2 weeks)

Secondary

MeasureTime frame
Foot Function IndexTimepoint: Pre-Treatment and Post-Treatment (After 2 weeks)

Countries

India

Contacts

Public ContactR Ravindran

All India Institute of Physical Medicine and Rehabilitation

rajaravindran@gmail.com9820264446

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026