Terminal Latency Index, Residual Latency and Median Ulnar F Latency Difference in Carpal Tunnel Syndrome

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

160 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-01-01

Study Completion Date

2016-03-02

Brief Summary

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Terminal latency index, residual latency and median ulnar F latency difference in carpal tunnel syndrome are specific parameters for the diagnosis

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Detailed Description

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Carpal tunnel syndrome is the most common compression neuropathy. This study was performed to determine the value of terminal latency index, residual latency and median ulnar F latency difference to investigate their sensitivity and specificity in the diagnosis of this syndrome.

We retrospectively determined the 160 patients. We evaluated the nerve conduction studies of patient and healthy arms. We recorded all nerve conduction study values.

Conditions

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Carpal Tunnel Syndrome

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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1

affected arms of patients who had gone to electrodiagnostic study and diagnosed as carpal tunnel syndrome

nerve conduction study

Intervention Type OTHER

nerve conduction study

2

healthy arms of patients who had gone to electrodiagnostic study and diagnosed as carpal tunnel syndrome in the other arms

nerve conduction study

Intervention Type OTHER

nerve conduction study

Interventions

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nerve conduction study

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients who had gone to electrodiagnostic study and diagnosed as carpal tunnel syndrome

Exclusion Criteria

* any history of hereditary polyneuropathies
* acquired polyneuropathies
* surgery or local steroid injections for upper limbs or effect the study
* any history of fracture at the sites of stimulation or recording

Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes