Patients are seen in Audiology for baseline and monthly serial audiologic analysis to determine whether or not Mevinolin has ototoxic side effects when administered in this manner over the prescribed period of time called for in the NHLBI study. Audiologic information on ototoxicity in this drug used in this manner is spotty and needs to be defined more accurately in this population. Thresholds for puretones and speech as well as suprathreshold measures of auditory function and electrophysiologic studies of the middle ear are included in the battery administered to this population. Data are being collected and will be analyzed for publication. To date (1 May 1985) 13 patients on the Mevinolin study have been seen with no subjects suffering significant ototoxic effect.

Agency
National Institute of Health (NIH)
Institute
Clinical Center (CLC)
Type
Intramural Research (Z01)
Project #
1Z01CL007006-02
Application #
4692004
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Clinical Center
Department
Type
DUNS #
City
State
Country
United States
Zip Code