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The effect of two shockwave focus and radial on the recovery of patients with carpal tunnel syndrome

Evaluation of the effect of focus shockwave and radial shockwave on the improvement of clinical symptoms and function in patients with carpal tunnel syndrome

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200825048515N38
Enrollment
40
Registered
2021-08-21
Start date
2021-08-22
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Carpal tunnel syndrome. Carpal tunnel syndrome

Interventions

Intervention 1: Intervention group 1: In this group, sham focus with radial shockwave (3000 shocks, intensity 3 bar and frequency HZ 10) in the carpal tunnel area is done one session per week for 3 we

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years Carpal tunnel syndrome with mild to moderate severity approved by a physician based on clinical examination and standard electrodiagnostic criteria Complete all treatment sessions (once a week for up to three weeks) consent to participate in the study

Exclusion criteria

Exclusion criteria: Severe carpal tunnel syndrome (Severe) Having diseases that mimic the symptoms of carpal tunnel syndrome, such as cervical radiculopathy, peripheral neuropathy, and median nerve trauma Pregnancy Having diabetes History of wrist fractures and dislocations History of hand surgery in the last 6 months Warfarin use or hereditary or acquired coagulation disorders Opioid use Taking herbal medicines and complementary medicine

Design outcomes

Primary

MeasureTime frame
Disease severity score. Timepoint: Before the intervention, three weeks and three months after the intervention. Method of measurement: The Boston Carpal Tunnel Questionnaire (BCTQ).

Secondary

MeasureTime frame
Functional status score. Timepoint: Before the intervention, three weeks and three months after the intervention. Method of measurement: The Boston Carpal Tunnel Questionnaire (BCTQ).;Pain. Timepoint: Before the intervention, three weeks and three months after the intervention. Method of measurement: The Boston Carpal Tunnel Questionnaire (BCTQ).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBabak Vahdatpour

Esfahan University of Medical Sciences

vahdatpour@med.mui.ac.ir+98 31 3620 2020

Outcome results

None listed

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