Skip to content

Shock wave therapy for treatment of chronic achilles tendinopathy.

Evaluating the effectiveness of extracorporeal shockwave therapy on pain reduction and function improvement in chronic achilles tendinopathy patients: a randomized clinical trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016051727907N1
Enrollment
40
Registered
2017-07-02
Start date
2015-03-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Achilles tendinopathy. Achilles tendinitis, unspecified leg.

Interventions

Intervention 1: Intervention group: 4 session of shock wave weekly. Focused: 1500, Energy: 0.25-0.4 Frequency: 2-3 HZ Radial: 3000, Energy: 1.8-2.6 Frequency: 21Hz In addition to conservative treatme
Intervention group: 4 session of shock wave weekly. Focused: 1500, Energy: 0.25-0.4 Frequency: 2-3 HZ Radial: 3000, Energy: 1.8-2.6 Frequency: 21Hz In addition to conservative treatment including:
Control group: 4 session of SHAM shock wave weekly. Focused: 1500, Energy:0 Frequency: 2-3 HZ Radial: 3000, Energy: 0 Frequency: 21Hz In addition to conservative treatment including: Therapeutic e

Sponsors

vice chancellor for research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: at least six months of pain and tenderness of the Achilles tendon; existence of a swollen and painful area on the Achilles tendon; having pain along with plantar flexion in the ankle; having pain in the exacerbated dorsiflexion condition in the ankle Exclusion criteria: Receiving extracorporeal shockwave lithotripsy during the past 6 months; Local injection of steroids during the past 3 months; Having associated diseases such as Polyneuropathy; Patient’s unwillingness to continue or lack of cooperation; using another type of treatment; changing the treatment plan based on the physician’s opinion

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Performance. Timepoint: Before intervention/ Immediately after, 1 month and 4 months after intervention. Method of measurement: The American Orthopedic Foot and Ankle Score.;Pain. Timepoint: Before intervention/ Immediately after, 1 month and 4 months after intervention. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHadi Foroozan

Isfahan University of Medical Sciences

hadi_foroozan@resident.mui.ac.ir+98 31 3668 5555

Outcome results

None listed

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