Skip to main content
Clinical Trials/NCT05157321
NCT05157321
Completed
Not Applicable

Effect of Repetitive Transcranial Magnetic Stimulation on Essential Tremors

Al-Azhar University1 site in 1 country30 target enrollmentDecember 10, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Essential Tremor
Sponsor
Al-Azhar University
Enrollment
30
Locations
1
Primary Endpoint
change in severity of essential tremors
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The aim of the study is to investigate the Effect of Repetitive Transcranial Magnetic Stimulation on Essential Tremors.

Detailed Description

Prior to start of rTMS sessions, Clinical evaluation and scaling of tremors using the ET rating scale (Fahn, Tolosa, Marin Tremor Rating Scale) will be employed on the participants in both groups. rTMS frequency of 1Hz will be delivered to each of the participants in both groups. Each session will be administered once daily for 3 days a week for 4 weeks. 1200 pulses (30 pulses per train with total 40 trains having inter-train delay of 3 seconds) per session will be provided with the coil placed on both cerebellar hemispheres. rTMS frequency of 1Hz was kept constant based on previous studies. rTMS sessions will be administered by trained professionals who was kept blinded to the research protocols used in the study. After completion of therapeutic programs (after 4 weeks), the participants will be asked to undergo post assessment of Fahn, Tolosa, Marin Tremor Rating Scale at the end of last rTMS session, 1 month, 3 months later.

Registry
clinicaltrials.gov
Start Date
December 10, 2021
End Date
April 30, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed Fathy Mohammed Mohammed

physician

Al-Azhar University

Eligibility Criteria

Inclusion Criteria

  • Patient diagnosed with Essential tremors or Essential tremors plus based on the movement disorders consensus criteria(appendix 1)
  • Patient should have significant residual tremors despite of using appropriate medical treatment.
  • Age: patient should be above 18 years old.
  • Gender: males and females.

Exclusion Criteria

  • Patients with history of seizures.
  • Patient receiving tremor active drugs including:
  • Central cholinergic drugs (acetylcholine chloride, muscarinic and nicotinic agonists, anticholinesterases, and aminopropranolols)
  • Central monoaminergic drugs (neuroleptics, phenylethylamines, and indoles)
  • Peripheral adrenergic drugs (lithium carbonate, amphetamine sulfate, adrenocorticosteroids, and thyroid hormone supplements)
  • Anticonvulsants (valproic acid), bronchodilators (theophylline and terbutaline sulfate)
  • Antidepressants (amitriptyline hydrochloride).
  • patients who have metal or electronic device implanted in their body such as :
  • cardiac peace maker
  • Aneurysm clips or coils

Outcomes

Primary Outcomes

change in severity of essential tremors

Time Frame: 1 day, 1 month, and 3 months following the end of treatment.

Fahn, Tolosa, Marin Tremor Rating Scale

Study Sites (1)

Loading locations...

Similar Trials