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Effect of Stellate Ganglion Block on Meniere's Disease

Effect of Stellate Ganglion Block on Meniere's Disease

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01574313
Enrollment
20
Registered
2012-04-10
Start date
2010-04-30
Completion date
2012-03-31
Last updated
2012-04-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Meniere Disease, Vertigo

Keywords

stellate ganglion block., Meniere's disease., electrocochleography., vertigo., hearing impairment.

Brief summary

Stellate ganglion block (SGB) has been the alternative treatment of Meniere's disease for years. However, objective evidence of the effect of SGB was still lack. The investigators conducted a randomized controlled study to examine the immediate effects of SGB in SP/AP of electrocochleography (ECoG).

Detailed description

Ten patients were randomly assigned to receive stellate ganglion block. These ten patients made up the experimental group. Another ten patients in the control group were assigned to receiving one dosage of oral medications: 0.25mg of erispan@ (fludiazine) , 25mg cephadol@ (diphenidol), and 200mg kentons@ (tocopherol nicotinate).

Interventions

PROCEDUREstellate ganglion block

stellate ganglion block

DRUG0.25mg, fludiazine

0.25mg of erispan@ (fludiazine), p.o. one dose only.

DRUG25mg cephadol@ (diphenidol)

25mg cephadol@ (diphenidol) p.o. one dose only.

DRUG200mg kentons@ (tocopherol nicotinate).

200mg kentons@ (tocopherol nicotinate) p.o. one dose only.

Sponsors

Chi Mei Medical Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* patients diagnosed with unilateral Meniere's disease, according to the criteria of the American Academy of Otolaryngology-Head and Neck Surgery, AAO-HNS (1995)

Exclusion criteria

* patients with coagulopathy, * arrhythmia, * myocardial ischemia, * glaucoma, * pregnant, * chronic otitis media or externa, and * past history of middle or inner ear surgery were excluded.

Design outcomes

Primary

MeasureTime frameDescription
SP/AP of ElectrocochleographyECoG was reorded 2 hours after SGBSP/AP of ECoG was recorded 2 hours after SGB. to be compared with the SP/AP of ECoG recorded before treatment

Secondary

MeasureTime frameDescription
SP/AP recorded at 4 hours after SGB4 hours after SGBSP/AP recorded at 4 hours after SGB was compared with that of pretreatment with SGB
SP/AP recorded at 6 hours after SGB6 hours after SGBSP/AP recorded at 4 hours after SGB was compared with the SP/AP recorded before SGB
scores of verbal scale for vertigo recorded at 6 hours after SGB6 hours after SGBscores of verbal scale for vertigo recorded at 6 hours after SGB was compared to the scores recorded before SGB

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026