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Effectiveness of high intensity laser therapy addition to conventional conservative treatment for carpal tunnel syndrome

Effectiveness of high intensity laser therapy addition to conventional conservative treatment for carpal tunnel syndrome compared with conventional conservative treatment alone in terms of clinical outcomes and electrophysiologic parameters: an experiment trial (non-randomized clinical trials) single blind study.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230103002
Enrollment
64
Registered
2023-01-03
Start date
2022-05-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

The patient was diagnosed with CTS with a minimal, mild, or moderate degree based on the modified neurophysiologic grading system. high intensity laser therapy, carpal tunnel syndrome, numbness, pain, electrophysiologic parameters

Interventions

the control group were treated with behavioral adjustments including wrist posture education for the workplace and daily life, avoid frequently flexing or moving the wrist
take only a vitamin B complex tablet three times daily
use wrist support with a 10-degree wrist extension during sleeping time.,The experimental group will maintain the same basics treatment as the control group but will add the HILT using Mectronic healt
Control group,High intensity laser therapy (HILT) group

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Study participants were adults (age greater than or equal 20 years); 2. presented with hand pain or numbness and underwent electrodiagnosis, and the result was minimal, mild, or moderate CTS levels based on the modified neurophysiologic grading system

Exclusion criteria

Exclusion criteria: 1) contraindication to laser such as undergoing cancer treatment, had radiation therapy during the past six month, and the patient had bleeding from the arm to the finger; 2) underlying disease that may cause the experimental measurements were disturbed such as polyneuropathy, cervical radiculopathy, brachial plexopathy, ulnar neuropathy, radial neuropathy, rheumatoid arthritis; 3) received conservative treatment within 6 months such as physical modality, orthosis and intracarpal tunnel steroid injection; 4) History of carpal tunnel release; 5) Numeric rating score of pain greater than or eqaul 8

Design outcomes

Primary

MeasureTime frame
numbness score 5 week at the end of the intervention numeric rating scale of numbness

Secondary

MeasureTime frame
pain score 5 week at the end of the intervention numeric rating scale of pain,Symptom of carpal tunnel syndrome 5 week at the end of the intervention Boston questionnaire,electrophysiologic parameter of median nerve 5 week at the end of the intervention electrodiagnosis study

Countries

Thailand

Contacts

Public ContactSucha Kumnoonsup

Saraburi hospital

sucha_k@hotmail.com0819274153

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026