- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05965791
Median Nerve Function During Phalen's Test
July 20, 2023 updated by: Mohamed Magdy ElMeligie, Ahram Canadian University
Electrophysiological Assessment of the Median Nerve During the Phalen's Test for Carpal Tunnel Syndrome
This study will use electromyography and nerve conduction studies to evaluate median nerve function during the Phalen's wrist flexion test in different wrist positions.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The Phalen's test is commonly used to assess carpal tunnel syndrome.
However, it is unclear which wrist position during this test best isolates median nerve function.
This study will measure thenar muscle activation and median nerve conduction in 30 healthy participants performing the Phalen's test.
Different wrist flexion angles will be evaluated to determine which position optimally targets the median nerve.
Results may enhance utilization of the Phalen's test in clinical practice and research.
Study Type
Observational
Enrollment (Estimated)
30
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
- Name: Mohamed M ElMeligie, Ph.d
- Phone Number: +201064442032
- Email: mohamed.elmeligie@acu.edu.eg
Study Locations
-
-
Giza
-
Al Ḩayy Ath Thāmin, Giza, Egypt, 3221405
- Recruiting
- Outpatient clinic of faculty of physical therapy, Ahram Canadian University
-
Contact:
- Mohamed M ElMeligie, Ph.d
- Phone Number: 01064442032
- Email: mohamed.elmeligie@acu.edu.eg
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Healthy men and women aged 18-45 recruited from the local community.
Description
Inclusion Criteria:
- Healthy adults aged 18-45 years
- No history of hand/wrist disorders
Exclusion Criteria:
- Contraindications to EMG or NCV
- Neurological or muscular disorders
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 |
|---|---|
|
Healthy Adults
30 healthy adult participants aged 18-45 years performing the Phalen's wrist flexion test
|
The Phalen's test will be performed at different wrist flexion angles from 0 to 90 degrees.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Thenar Muscle Activation
Time Frame: Baseline
|
Mean EMG activity of the thenar muscles during the Phalen's test at different wrist angles.
Measured in microvolts (μV).
|
Baseline
|
|
Median Nerve Conduction Velocity during Phalen's Test
Time Frame: Baseline
|
Median nerve conduction velocity (measured in meters per second, m/s) assessed using surface electrodes at the wrist and elbow during the Phalen's test wrist flexion maneuver.
Measured bilaterally at each wrist flexion angle during a single study visit.
|
Baseline
|
|
Median Nerve Distal Latency during Phalen's Test
Time Frame: Baseline
|
Median nerve distal latency (measured in milliseconds, ms) assessed using surface electrodes over the abductor pollicis brevis and stimulating the median nerve at the wrist during the Phalen's test.
Measured bilaterally at each wrist flexion angle during a single study visit.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Amal Fawzy, Ph.d, Faculty of Physical Therapy, Ahram Canadian University
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 (Estimated)
July 25, 2023
Primary Completion (Estimated)
November 25, 2023
Study Completion (Estimated)
December 15, 2023
Study Registration Dates
First Submitted
July 20, 2023
First Submitted That Met QC Criteria
July 20, 2023
First Posted (Actual)
July 28, 2023
Study Record Updates
Last Update Posted (Actual)
July 28, 2023
Last Update Submitted That Met QC Criteria
July 20, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OT-PT-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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