- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03300856
Chart Review: Central Motor Conduction Time in Neurological Disorders
Background:
TMS stands for transcranial magnetic stimulation. It is a non-invasive way to stimulate the brain. It helps researchers study the nervous system. TMS can assess central motor conduction time (CMCT). That can be used to diagnose some diseases. It can also show how well treatments are working. Researchers want to study the records of people who have already had TMS. They want to see how it relates to the results of diagnostic studies.
Objectives:
To study the results of transcranial magnetic stimulation in certain neurological disorders. To create a descriptive analysis of the results.
Eligibility:
Records that are already in the NINDS database
Design:
The study will not enroll any participants.
Researchers will search the database for certain terms. These include TMS, CMTC, and motor evoked potentials. This will identify records of people who had TMS for diagnosis.
Using data from the records, researchers will calculate CMCT. They will note other data that relate to CMCT.
Researchers will analyze their findings. They will write a review article.
Personal data will be removed from all the records before the findings are analyzed.
Study Overview
Status
Conditions
Detailed Description
Objective- To retrospectively study the results of transcranial magnetic stimulation (TMS) in various neurological disorders and create a descriptive analysis of the results.
Study population- Existing records of patients within the NINDS database who have had TMS performed to measure central motor conduction time (CMCT).
Design-
- Retrospective descriptive analysis.
- The NINDS EMG Database will be queried using terms such as TMS, CMCT, and MEP (motor evoked potentials) to identify EMG reports on patients who underwent TMS for diagnosis
- Within these reports peripheral motor conduction time (PMCT), the cortical motor evoked potential (MEP) latency and amplitude will be used to calculate CMCT, clinical patient factors pertinent to estimation of CMCT as well clinically significant physical exam findings will be recorded as well.
- Clinical diagnoses and neurological exams will be extracted from medical records
- Patient identifiers will be de-linked after compiling data from medical records
Outcome measures
- Results of CMCT using TMS in different diagnoses will be summarized for different neurologic disorders and correlated to clinical exam measures documented in previous records
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Maryland
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Bethesda, Maryland, United States, 20892
- National Institute of Neurological Disorders and Stroke (NINDS)
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
INCLUSION CRITERIA:
- Patients who were seen in the NINDS EMG section for diagnostic TMS studies
- Patients tested between 1998 and 2017
- Greater than or equal to age 18.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
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Chart Review
Existing records of patients within the NINDS database who have had TMS performed to measure central motor conduction time (CMCT).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Summary of central motor conduction studies in neurological disorders
Time Frame: Study completion
|
Study completion
|
Collaborators and Investigators
Investigators
- Principal Investigator: Mary Kay Floeter, M.D., National Institute of Neurological Disorders and Stroke (NINDS)
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 999917170
- 17-N-N170
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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