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tDCS for Laryngeal Dystonia

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Yale University

Status

Enrolling

Conditions

Laryngeal Dystonia

Treatments

Device: Starstim system

Study type

Interventional

Funder types

Other

Identifiers

NCT06830174
2000032414

Details and patient eligibility

About

This project will apply transcranial direct current stimulation (tDCS) to multiple brain areas to evaluate the effects as a potential treatment for laryngeal dystonia (formerly spasmodic dysphonia).

Full description

Baseline neuroimaging data will be acquired from all participants via MRI, EEG. Each participant will be seen for multiple testing sessions over a five day period. LD participants will undergo the neuromodulation (HD-tDCS Stimulation) for twenty minutes while engaged in watching videos/movies or performing a word production task.

Enrollment

10 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants must be clinically evaluated for the diagnosis of LD or have the proof of LD diagnosis. (Not applicable for control participants)
  • No other known or history of speech, voice disorder other than LD.
  • Provision of signed and dated informed consent form.
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Must not be pregnant.

Exclusion criteria

  • All individuals who do not meet the above mentioned criteria are excluded from the study.
  • Subjects with a history of epilepsy or depression or is claustrophobic.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Laryngeal Dystonia (LD) tDCS
Experimental group
Description:
Adductor, Abductor and Mixed type LD with clinical evaluation of LD or with proof of LD diagnosis
Treatment:
Device: Starstim system

Trial contacts and locations

1

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Central trial contact

Nabin Koirala, PhD

Data sourced from clinicaltrials.gov

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