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The Efficacy of Laser Therapy and Radial Shock Wave Therapy in Carpal Tunnel Syndrome patients

Comparison Between Efficacy of Laser Therapy and Radial Shock Wave Therapy on Pain, Grip Strength and Function in Patient with Carpal Tunnel Syndrome: A Randomized Clinical Trial - NIL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070547
Enrollment
34
Registered
2024-07-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: G560- Carpal tunnel syndrome

Interventions

Intervention1: LASER Therapy: LASER Therapy 10 sessions (5 sessions per week for 2 weeks) along with Standardized Exercise Program and Home Exercise Program (5 sessions per week for 2 weeks) Control I

Sponsors

Yadul Saikh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Both male and female patients. 2.Age group between 30 to 60 years. 3.Clinical symptoms, such as night pain, numbness, and tingling sensation on the median nerve distribution over the hand or both hand that have persisted for more than 1 months. 4.VAS score between 3 cm to 7 cm. 5.Any one of following special test should be positive; a.Phalens test b.Tinel sign c.Carpal compression test 6.Carpal Tunnel Syndrome confirmed by Nerve conduction velocity (NCV).

Exclusion criteria

Exclusion criteria: 1.Musculoskeletal conditions like rheumatoid arthritis, upper limb fracture, hand deformity etc. 2.Disorders that mimic CTS, such as cervical radiculopathy, polyneuropathy, and thoracic outlet syndrome etc. 3.Metabolic disorders like acromegaly. 4.History of corticosteroid injections in last 3 months or oral steroids in last 1months. 5.Surgical history involving the wrist. 6.Neurological conditions like Stroke, Complex regional pain syndrome (CRPS), Parkinson’s disease etc. 7.Pregnancy.

Design outcomes

Secondary

MeasureTime frame
NILTimepoint: NIL

Primary

MeasureTime frame
1.Pain intensity by VAS 2.Maximum Grip strength by Hand-Held Dynamometer 3.Hand Function by BCTS Questionnaire Timepoint: 2 times -on day 0 and after 10 days of intervention

Countries

India

Contacts

Public ContactYadul Saikh

National Institute for Locomotor Disabilities (Divyangjan)

drpravinkumar@gmail.com9815365870

Outcome results

None listed

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