Spasmodic dystonia

disease
On this page

Also known as abductor spasmodic dysphoniaadductor spasmodic dysphonialaryngeal dyskinesialaryngeal dystoniamixed spasmodic dysphonia (type)spasmodic dysphoniaspastic dysphonia

Summary

Spasmodic dystonia (MONDO:0000485) is a disease and 40 clinical trials. Top therapeutic interventions include oxybate, pyridostigmine, and daxibotulinumtoxina. A subtype of focal dystonia — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 40

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namespasmodic dystonia
Mondo IDMONDO:0000485
MeSHD055154
Orphanet93961
DOIDDOID:0050844
SNOMED CT3331000119108
UMLSC1963946
MedGen409603
GARD0027260
Is cancer (heuristic)no

Also known as: abductor spasmodic dysphonia · adductor spasmodic dysphonia · laryngeal dyskinesia · laryngeal dystonia · mixed spasmodic dysphonia (type) · spasmodic dysphonia · spastic dysphonia

Disease family

This is a subtype of focal dystonia. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › nervous system disordermovement disorderextrapyramidal and movement diseasedystonic disorderfocal dystoniaspasmodic dystonia

Related subtypes (11): anismus, cervical dystonia, focal hand dystonia, oculogyric crisis, craniofacial dystonia, X-linked dystonia-parkinsonism, torsion dystonia 7, benign essential blepharospasm, dystonia 23, oromandibular dystonia, dystonia, focal, task-specific

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

Drugs indicated or in trials for this disease

No drug has an approved disease-direct ChEMBL indication for this disease.

1 drug in clinical trials for this disease (phase 2–3, investigational): efficacy not established — a trial record, not an indication.

DrugHighest phase
LidocainePhase 2

Clinical trials & evidence

Clinical trials

Clinical trials: 40.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified27
PHASE2/PHASE33
PHASE23
PHASE1/PHASE23
PHASE12
PHASE41
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05110417PHASE4UNKNOWNReversal of Botulinum Neurotoxin Injection Related Dysphonia With Pyridostigmine
NCT02528006PHASE2/PHASE3COMPLETEDTreatment for Adductor Spasmodic Dysphonia by Type 2 Thyroplasty Using Titanium Bridges
NCT03292458PHASE2/PHASE3COMPLETEDSodium Oxybate in Spasmodic Dysphonia and Voice Tremor
NCT04648891PHASE2/PHASE3COMPLETEDSpasmodic Dysphonia Pain
NCT05892770PHASE1/PHASE2ACTIVE_NOT_RECRUITINGZinc Supplementation Prior to Botox Injections for Spasmodic Dysphonia
NCT01961297PHASE2COMPLETEDVoice Tremor in Spasmodic Dysphonia: Central Mechanisms and Treatment Response
NCT04938154PHASE2UNKNOWNA Phase 2 Trial of Deep Brain Stimulation for Spasmodic Dysphonia
NCT05158166PHASE1/PHASE2COMPLETEDDaxibotulinumtoxinA Injection for Treatment of Adductor Spasmodic Dysphonia
NCT05467228PHASE2WITHDRAWNLaryngeal Vibro-tactile Stimulation as a Non-invasive Symptomatic Treatment for Spasmodic Dysphonia
NCT06111027PHASE1/PHASE2COMPLETEDUsability of Vibro-tactile Stimulation to Treat Spasmodic Dysphonia
NCT07041203PHASE1NOT_YET_RECRUITINGExtended-release Sodium Oxybate (Lumryz) in Spasmodic Dysphonia and Voice Tremor
NCT00015795PHASE1COMPLETEDStudy of Air Stream in Voice Production
NCT05216770EARLY_PHASE1RECRUITINGUnderstanding Disorder-specific Neural Pathophysiology in Laryngeal Dystonia and Voice Tremor
NCT03042962Not specifiedRECRUITINGBrain Networks in Dystonia
NCT03042975Not specifiedRECRUITINGImaging Genetics of Laryngeal Dystonia
NCT04421365Not specifiedRECRUITINGBrain-Computer Interfaces in Laryngeal Dystonia
NCT05095740Not specifiedRECRUITINGEffects of Neuromodulation in Laryngeal Dystonia
NCT05150093Not specifiedRECRUITINGDeep Brain Stimulation in Laryngeal Dystonia and Voice Tremor
NCT05150106Not specifiedRECRUITINGCharacterization of Clinical Phenotypes of Laryngeal Dystonia and Voice Tremor
NCT05245942Not specifiedACTIVE_NOT_RECRUITINGMonitoring of the Safety and the Performance of the Endoscopic Cap Electrode (ECE50)
NCT05506085Not specifiedRECRUITINGDeep Brain Stimulation for Laryngeal Dystonia: From Mechanism to Optimal Application
NCT06078527Not specifiedNOT_YET_RECRUITINGAssessment of Laryngopharyngeal Sensation: Cancer Survivor Cohort
NCT06561334Not specifiedACTIVE_NOT_RECRUITINGSpasmodic Dysphonia Interviews
NCT06830174Not specifiedRECRUITINGtDCS for Laryngeal Dystonia
NCT07443891Not specifiedRECRUITINGBrain Network Changes After Vibro-tactile Stimulation in Laryngeal Dystonia
NCT00001552Not specifiedCOMPLETEDCharacteristics of Idiopathic Familial Voice Disorders
NCT00001922Not specifiedCOMPLETEDSensory Function in Idiopathic Voice Disorders
NCT00118586Not specifiedCOMPLETEDNeuropathology of Spasmodic Dysphonia
NCT00713414Not specifiedCOMPLETEDRole of Neurotransmission and Functional CNS Networks in Spasmodic Dysphonia
NCT00895063Not specifiedTERMINATEDEffect of Vocal Exercise After Botulinum Toxin Injection for Spasmodic Dysphonia
NCT02061943Not specifiedWITHDRAWNExamining the Spasmodic Dysphonia Diagnosis and Assessment Procedure (SD-DAP) for Measuring Symptom Change
NCT02558634Not specifiedCOMPLETEDThalamic Deep Brain Stimulation for Spasmodic Dysphonia- DEBUSSY Trial
NCT02957942Not specifiedCOMPLETEDrTMS in Spasmodic Dysphonia
NCT03129087Not specifiedUNKNOWNThe Effect of Vocal Rest Versus Vocalization Following Xeomin® Injections in Spasmodic Dysphonia
NCT03349086Not specifiedCOMPLETEDEffects of Vocal Exercises for Spasmodic Dysphonia
NCT03746509Not specifiedCOMPLETEDLaryngeal Vibration for Spasmodic Dysphonia
NCT05158179Not specifiedCOMPLETEDAssessment of Laryngopharyngeal Sensation in Adductor Spasmodic Dysphonia
NCT05580302Not specifiedUNKNOWNCortical Silent Period in Laryngeal Dystonia
NCT06402214Not specifiedUNKNOWNThe ‘Lombard Effect’ in Patients Affected by Adductor Laryngeal Dystonia
NCT06767215Not specifiedCOMPLETEDDysphonia Pain Perception Following Botulinum Toxin Injections

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
OXYBATE49
PYRIDOSTIGMINE42
DAXIBOTULINUMTOXINA41
LIDOCAINE41