Role of Ultrasonography in the Diagnosis of Carpal Tunnel Syndrome

August 13, 2021 updated by: Mostafa Ahmed Mohamed, Sohag University

Role of Ultrasonography in the Diagnosis of Carpal Tunnel Syndrome and Detection of Its Severity

This prospective study aims to evaluate the median nerve in Carpal Tunnel Syndrome by high-frequency ultrasound and color Doppler in comparison with clinical and Nerve conduction studies.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

This prospective study aims to evaluate the median nerve anatomical changes in Carpal Tunnel Syndrome by high-frequency ultrasound and color Doppler in comparison with clinical and Nerve conduction studies physiological changes to determine the efficacy of ultrasound to diagnose and determine the severity of carpal tunnel syndrome.

Study Type

Observational

Enrollment (Anticipated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Sohag, Egypt, 82524
        • Recruiting
        • Sohag University - Faculty of Medicine
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

sohag university hospital patients and attendants

Description

Inclusion Criteria:

  • Any Age Group with symptoms, clinical signs and NCS consistent with CTS

Exclusion Criteria:

  • Uncooperative Patients .
  • Patients with History of previous wrist surgery, fracture or traumatic nerve injury

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
patients
those with symptoms of CTS
imaging by ultrasonography and nerve conduction studies will be done for both grups
Other Names:
  • nerve conduction studies
control group
normal people those with no symptoms of CTS
imaging by ultrasonography and nerve conduction studies will be done for both grups
Other Names:
  • nerve conduction studies

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
anatomical changes in the median nerve in carpal tunnel syndrome
Time Frame: imaging within 24 hours from the nerve conduction studies and clinical assessment of the patient
compare the anatomical changes observed by ultrasonography in patients diagnosed with carpal tunnel syndrome and comparing the results with clinical and nerve conduction studies results
imaging within 24 hours from the nerve conduction studies and clinical assessment of the patient

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: mostafa mm mohamed, MBBCH, Sohag University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

August 29, 2021

Primary Completion (Anticipated)

February 2, 2022

Study Completion (Anticipated)

March 20, 2022

Study Registration Dates

First Submitted

July 15, 2021

First Submitted That Met QC Criteria

July 15, 2021

First Posted (Actual)

July 26, 2021

Study Record Updates

Last Update Posted (Actual)

August 17, 2021

Last Update Submitted That Met QC Criteria

August 13, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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