Essential Tremor in Children and Adolescent
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|ClinicalTrials.gov Identifier: NCT03487705|
Recruitment Status : Not yet recruiting
First Posted : April 4, 2018
Last Update Posted : July 16, 2018
|Condition or disease||Intervention/treatment||Phase|
|Essential Tremor||Other: electromyographic essential tremor||Not Applicable|
A multicenter, descriptive cross-sectional study will include children and adolescents whose diagnosis of TE has been retained by an abnormal movement specialist before the age of 18 years.
Each child will benefit from an examination and a neurological and general clinical examination, a functional questionnaire, an electromyogram with accelerometer.
Will be determined: demographic characteristics (age, sex and ethnicity), family history of essential tremor, age of onset of tremor, tremor characteristics (location, occurrence conditions, aggravating or precipitating factors, scalability); additional examinations carried out and the treatments proposed or taken by the child as well as the functional repercussions of TE in the child.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||35 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Clinical and Electrophysiological Characterization of Essential Tremor in Children and Adolescents|
|Estimated Study Start Date :||October 1, 2018|
|Estimated Primary Completion Date :||May 1, 2019|
|Estimated Study Completion Date :||November 1, 2019|
child essential tremor
electromyogram with accelerometer
Other: electromyographic essential tremor
Making a recording electromyographic essential tremor in each child
- characteristics of TE [ Time Frame: 1 day ]échelle Fahn-Marin- Tolosa FMT
- determine the electrophysiological characteristics impact of TE functional questionnaire, an electromyogram with accelerometer. [ Time Frame: 1 day ]electromyogram with accelerometer
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03487705
|Contact: Agathe ROUBERTIE, Pr||04 67 33 01 email@example.com|
|Contact: Guillemette TACONNET DECKER|
|Principal Investigator:||Agathe ROUBERTIE, Pr||University Hospital, Montpellier|