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Median Nerve Strain and Applied Pressure Measurement in the Carpal Tunnel Syndrome Patients

Median Nerve Strain and Applied Pressure Measurement in the Carpal Tunnel Syndrome Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04027998
Enrollment
100
Registered
2019-07-22
Start date
2015-04-03
Completion date
2024-12-31
Last updated
2022-04-27

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

Conditions

Carpal Tunnel Syndrome

Brief summary

The aim of this study is to investigate diagnostic accuracy of median nerve strain and applied pressure measurement . Idiopathic carpal tunnel syndrome patients and healthy controls will be evaluated by ultrasound. Median nerve strain, pressure applied to the skin will be measured at the proximal part of the carpal tunnel. The parameters will be compared between patients and controls, and before and after the open carpal tunnel release in the patients.

Detailed description

The aim of this study is to investigate diagnostic accuracy of median nerve strain and applied pressure measurement . Idiopathic carpal tunnel syndrome patients and healthy controls will be evaluated by ultrasound. Median nerve strain, pressure applied to the skin, and ratio of pressure-strain will be measured at the proximal part of the carpal tunnel. In addition, distal latencies in the motor and sensory nerve conductions studies and cross-sectional area of median nerve will be measured. The parameters will be compared between patients and controls, and before and after the open carpal tunnel release in the patients.

Interventions

DIAGNOSTIC_TESTstrain and applied pressure measurement

Measurement of median nerve strain and applied pressure at proximal carpal tunnel level

Sponsors

Tokyo Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* carpal tunnel syndrome patients and asymptomatic control

Exclusion criteria

* Patients were excluded if there was a history of cervical radiculopathy, rheumatoid arthritis, gout, hemodialysis, sarcoidosis, amyloidosis, or traumatic injuries to the arm. Written consent was obtained from all study participants

Design outcomes

Primary

MeasureTime frameDescription
median nerve strainthrough study completion, an average of 1 yearChange of the median nerve strain from the initial measurement at 3, 6, 12 months after the treatment
applied pressurethrough study completion, an average of 1 yearChange of the applied pressure from the inital measurement at 3, 6, 12months after the treatment

Countries

Japan

Contacts

Primary ContactYuichi Yoshii
yy12721@yahoo.co.jp81298871161

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026