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Multiscent Digital Olfactory Identification Test

Overview

About this study

The purpose of this study is to test the validity of Multiscent in the USA population by studying the correlation and agreement between Multiscent and UPSIT results in normosmic, hyposmic, and anosmic subjects.

 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Adults aged 18 years or older. 
  • United States resident (have lived in the US for at least 1 year)
  • Self-reported preserved sense of smell (for the normosmia group). 
  • Complaints of olfactory disturbances (for the hyposmia and anosmia group). 

Exclusion Criteria:

  • History of nasosinusal tumor. 
  • Symptoms of a cold, acute sinusitis, or flu on the day of the exam or the day before. 
  • Illiteracy or reading difficulties.
  • Ongoing pregnancy

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 07/18/2024. Questions regarding updates should be directed to the study team contact.

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Devyani Lal, M.D.

Open for enrollment

Contact information:

Pedro Gomes M.D.

(480) 342-2690

LancaGomes.Pedro@mayo.edu

More information

Publications

Publications are currently not available

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CLS-20584996

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