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Evaluation of the effect of interventions near and far to the carpal tunnel using dry needle method and routine physiotherapy

Evaluation of the effect of interventions near and far to the carpal tunnel site using dry needle method and routine physiotherapy on clinical and paraclinical indicators of patients with carpal tunnel syndrome (CTS)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130612013651N4
Enrollment
45
Registered
2020-07-23
Start date
2020-08-04
Completion date
Unknown
Last updated
2020-08-17

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: Dry needle intervention group: In this group, patient receives dryneedle for 20 minutes. Dry needling is performed on the muscles of Palmaris longus, pronator of fear, flexor digitrom,

Sponsors

Vice Chancellor for Research, Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Having clinical signs to diagnose carpal tunnel syndrome. Have symptoms of the disease in the last 6 months. Age range 20 to 65 years.

Exclusion criteria

Exclusion criteria: Pregnancy. Having a history of carpal tunnel syndrome hand surgery. systemic diseases. Therapeutic intervention has been performed in the last 6 months.

Design outcomes

Primary

MeasureTime frame
Median nerve conduction velocity. Timepoint: Before and after the intervention and one month follow-up interval. Method of measurement: electromyography device.;Muscle and fascia thickness. Timepoint: Before and after the intervention and follow-up interval. Method of measurement: sonography.

Secondary

MeasureTime frame
Pain intensity. Timepoint: Before and after the intervention and follow-up interval. Method of measurement: Visual analoug scale.;Functional ability. Timepoint: Before and after the intervention and follow-up interval. Method of measurement: Boston Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Barzegar

Yazd University of Medical Sciences

barzegarali66@gmail.com+98 35 3827 6825

Outcome results

None listed

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