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The effectiveness of peripheral magnetic stimulation combined with conventional therapy in moderate degree carpal tunnel syndrome : a randomized, assessor blinded, controlled trial

The effectiveness of peripheral magnetic stimulation combined with conventional therapy in moderate degree carpal tunnel syndrome : a randomized, assessor blinded, controlled trial

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230405001
Enrollment
60
Registered
2023-04-05
Start date
2023-06-01
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

Moderate degree of carpal tunnel syndrome carpal tunnel syndrome peripheral magnetic stimulation conventional therapy electrodiagnosis

Interventions

Peripheral magnetic stimulation - Transducer : 3 Tesla round coil - Protocol : frequency 10 Hz, On time 2 secs/train, Off time 2 secs/train, total 20 min/session - Site : along tract of median nerve f
Peripheral magnetic stimulation combined with conventional therapy,Conventional therapy

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age 20-80 years 2.Moderate to severe degree CTS by electrodiagnostic study 3.Willing to participate in the study

Exclusion criteria

Exclusion criteria: 1.Electrodiagnosis reveals : Absent SNAP, absent CMAP or CMAP amplitude <5 mV 2.History of treatment of carpal tunnel syndrome by steroid injection < 6 months, physical modalities within 1 month, using NSAIDs drug within 2 week, using wrist splint within 3 month or had already underwent carpal tunnel surgery 3.Contraindication for peripheral magnetic stimulation : Pregnancy, Active malignancy, Epilepsy, Pacemaker, Intracranial/spinal metal object, Cochlear implant, History of wrist fracture at affected side, DVT at affected arm 4.Diagnosed as cervical radiculopathy, polyneuropathy, inflammatory rheumatoid, diabetes neuropathy or poor controlled diabetes mellitus 5.Cannot tolerate the wrist splint 6.Severe perception and communication impairment

Design outcomes

Primary

MeasureTime frame
Median nerve conduction study at 0,4,8 weeks after treatment Electrodiadnostic study

Secondary

MeasureTime frame
Pain and hand function at 0,4,8 weeks after treatment Thai boston carpal tunnel questionnaire

Countries

Thailand

Contacts

Public ContactPemika Khruarut

Faculty of medicine, Chulalongkorn university

pemika.khruarut@hotmail.com0858850508

Outcome results

None listed

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