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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01459692
Other study ID # HR15863
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2005
Est. completion date January 2008

Study information

Verified date May 2018
Source Medical University of South Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Neurologically-impaired individuals may have significant neurologic morbidity related to epilepsy and seizure disorders. Finding safe, noninvasive methods of decreasing seizures, and potentially reversing the epileptogenic process, is of paramount importance in improving the lives of those with epilepsy.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 2008
Est. primary completion date January 2008
Accepts healthy volunteers No
Gender All
Age group 5 Years to 90 Years
Eligibility Inclusion Criteria:

- Resident of Thad E. Saleeby Center

- Epilepsy or seizure disorder

- At least one year of detailed seizure reporting prior to study starting date

Exclusion Criteria:

- Severe hearing impairment

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Music Exposure
Twenty-seven subjects were randomly assigned to receive nightly exposure to music at periodic intervals between the hours of 9:00 PM and 8:00 AM.

Locations

Country Name City State
United States Medical University of South Carolina Charleston South Carolina

Sponsors (2)

Lead Sponsor Collaborator
Medical University of South Carolina MIND Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in seizure rates Main Outcome Measure: The effect of exposure to the auditory stimulus on seizure frequency. Changes in seizure rates from baseline to treatment years were determined and statistically compared within the treatment and control groups, as well as between the groups to assess efficacy of treatment. 3 years
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