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Superior laryngeal nerve block for laryngeal sensory neuropathy

Phase 2
Not yet recruiting
Conditions
Vocal cord dysfunction
aryngeal sensory neuropathy
Chronic Cough
Laryngeal sensory neuropathy
Respiratory - Other respiratory disorders / diseases
Registration Number
ACTRN12619000237189
Lead Sponsor
Department of Otolaryngology, Head and Neck surgery, Monash Health
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not yet recruiting
Sex
All
Target Recruitment
352
Inclusion Criteria

No objective evidence on formal testing and/or failure of adequate treatment to more common causes of treatment:
Respiratory Disease:
- Negative Testing: CXR or CT Chest, Broncho-provocation or Broncho-dilation testing
- No response to an 8 week empirical trial of inhaled corticosteroid
Allergic Disease:
- Negative Testing: Negative RAST or Skin prick testing for inhaled allergens
- No response to an 8 week empirical trial of intranasal and/or oral medications (e.g. Steroid, and/or Anti-histamine)
Laryngopharyngeal and Gastro-oesophageal Reflux Disease:
- Negative Testing: Negative Oral Salivary pepsin assay, or 24 hour dual probe pH/impedance monitoring.
- No response to an 8 week empirical trial of both acid reduction and alginate treatment.

Exclusion Criteria

Are on neuromodulator medications (ie. Tricyclic anti-depressants, SSRIs, Gabapentinoids)
Are on anti-tussive medications (ie Guafenasin)
Cannot tolerate an ‘in-office’ procedure
Known allergy or intolerance to bupivacaine and/or triamcinolone acetate

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in symptom scores on vocal cord dysfunction questionnaire[3 months];Change in symptom scores on cough severity index[3 months]
Secondary Outcome Measures
NameTimeMethod
change in symptom scores on vocal cord dysfunction questionnaire[12 months];change in symptom scores on cough severity index[12 months]
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