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The comparative evaluation of the effects of TECAR therapy and conventional physical therapy treatments on pain and function in people with Carpal tunnel syndrome

The comparative evaluation of the effects of TECAR therapy and conventional physical therapy treatments on pain and function in people with Carpal tunnel syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230724058902N1
Enrollment
44
Registered
2023-07-29
Start date
2023-07-31
Completion date
Unknown
Last updated
2023-08-21

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: 10 sessions routine physiotherapy - 5 minutes of non-continuous ultrasound (1:4) (manufactured by Novin Medical Engineering Company, model 215M) with a frequency o

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 65 Years

Inclusion criteria

Inclusion criteria: Moderate to severe carpal tunnel syndrome based on electrodiagnostic findings 25-65 years old people Tingling pain with pins and needle sensation and numbness in thumb, index, middle and radial half of ring finger Presence of symptoms more than 3 months

Exclusion criteria

Exclusion criteria: Metabolic and systemic disorder: hypothyroidism, diabetes, rheumatoid arthritis Polyneuropathy Corticosteroid injection in the subject hand in the past 3 months Trauma history to the subject hand in past 12 months Past carpal tunnel syndrome surgery history in the affected hand Pace maker Severe neurologic disorder Pregnancy in study process Deformity in wrist or hand

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Beginning, after 10 sessions and 4 weeks later. Method of measurement: NPRS.;Function. Timepoint: Beginning, after 10 sessions and 4 weeks later. Method of measurement: Boston questionnaire.;Hand grip strength. Timepoint: Beginning, after 10 sessions and 4 weeks later. Method of measurement: Dynamometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNavid Taheri

Esfahan University of Medical Sciences

n_taheri@mui.ac.ir+98 13 3792 5049

Outcome results

None listed

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