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IMS-treatment and Canalis Carpi Syndrome

N

NORCE Norwegian Research Centre AS

Status

Completed

Conditions

Carpal Tunnel Syndrome

Treatments

Device: IMS of the musculus pronator teres
Device: Needle in acupuncture point Li11

Study type

Interventional

Funder types

Other

Identifiers

NCT01102868
IMS1234

Details and patient eligibility

About

Carpal tunnel syndrome is a condition in which the median nerve is compressed at the wrist, leading to paresthesias, numbness and muscle weakness in the hand. Treatment of the condition often involves surgery.

In this study we wish to se if there is an effect of using intramuscular stimulation (IMS) to release the tension of nervus medianus in the lower arm. The study will be performed by randomization to IMS of musculus pronator teres or a control ("Scam IMS treatment" to the acupuncture point Li11). The two insertion points are approximately 1cm apart in the lower arm.

Full description

The most important outcome measure is ultra sound measured diameters for nervus medianus in the carpal tunnel

Enrollment

75 patients

Sex

All

Ages

18 to 67 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Canalis Carpi Syndrome verified by ultrasound and clinically
  • Both genders
  • Age from 18 to 67

Exclusion criteria

  • Negative neurophysiology result.
  • Epilepsy,
  • Heart disease,
  • Rheumatism
  • Unstable angina pectoris,
  • Metal -allergy,
  • Needle- phobia,
  • Infection
  • Hemophilia
  • Cognitive problems

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

75 participants in 2 patient groups

Needle in acupuncture point Li11
Sham Comparator group
Description:
Acupuncture needle in the acupuncture point Li11
Treatment:
Device: Needle in acupuncture point Li11
IMS of musculus pronator teres
Experimental group
Description:
Acupuncture needle in musculus pronator teres
Treatment:
Device: IMS of the musculus pronator teres

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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