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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04727177
Other study ID # SAHZhejiangU2
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date November 1, 2020
Est. completion date May 1, 2021

Study information

Verified date January 2021
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Jianhua Feng
Phone 89713749
Email 380028654@qq.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this scheme, TMS treatment of Primary dystonia is planned by precise magnetic resonance positioning.


Recruitment information / eligibility

Status Recruiting
Enrollment 1
Est. completion date May 1, 2021
Est. primary completion date April 1, 2021
Accepts healthy volunteers No
Gender Male
Age group N/A and older
Eligibility Inclusion Criteria: - Primary dystonia Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Transcranial magnetic stimulation
Transcranial magnetic stimulation (TMS) is a noninvasive biological stimulation technique born in the middle of 1980's.

Locations

Country Name City State
China Zhejiang University Hangzhou Zhejiang

Sponsors (2)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Normal University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Burke-Fahn-Marsden dystonia rating scale The BFMMS measures dystonia in nine body regions (including the eyes, mouth, speech and swallowing, neck, trunk, arms, and legs) with scores ranging from 0 (minimum) to 120 (maximum).The higher scores mean a worse outcome.
The BFMDS is a functional marker consisting of parental- or self-reported daily activities (involving speech, handwriting,feeding, eating, swallowing, hygiene, dressing, and walking),with scores ranging from 0 (completely independent) to 30 (completely dependent).
Five days
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