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The Effect of Laser Therapy on Carpal Tunnel Syndrome

The Effect of High-Power and Low-Power Lasers on Symptoms and the Nerve Conduction Study in Patients With Carpal Tunnel Syndrome. A Prospective Randomized Single-Blind Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201130049543N1
Enrollment
65
Registered
2020-12-12
Start date
2018-01-01
Completion date
Unknown
Last updated
2021-01-05

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: Control group: Wrist splint prescription. A wrist splint with a volar metal bar was used at an angle of 0° for 12 weeks. The patients were instructed to wear the splint during the nigh

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients from 30-50 years of age Duration of symptoms for at least 3 months

Exclusion criteria

Exclusion criteria: The presence of other neuropathic diseases such as polyneuropathy, cervical radiculopathy, or brachial plexopathy (including thoracic outlet syndrome) Systemic diseases that can affect the severity or treatment, such as hypothyroidism, gout, systemic lupus erythematosus, rheumatoid arthritis, diabetes mellitus, chronic kidney deficiency, and acromegaly, History of carpal tunnel release surgery, Wrist fracture Pregnancy History of injectionin the carpal tunnel in the last month.

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before the treatment and immediately and 12 weeks after the last treatment session. Method of measurement: Visual analogue scale (VAS).

Secondary

MeasureTime frame
Grip strenghth. Timepoint: Before the treatment and immediately and 12 weeks after the last treatment session. Method of measurement: Manual dynamometer.;Median nerve conduction study. Timepoint: Before the treatment and immediately and 12 weeks after the last treatment session. Method of measurement: Electrodiagnosis test, by EMG-NCS devices.;Symptoms and function. Timepoint: Before the treatment and immediately and 12 weeks after the last treatment session. Method of measurement: Boston questionnair.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Fateme Hojjati

Shahid Beheshti University of Medical Sciences

Fatemehojjati@yahoo.com+98 21 2273 1112

Outcome results

None listed

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