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Legionnaires' Effect on Smell

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University of Pennsylvania

Status

Completed

Conditions

Legionnaires' Disease

Treatments

Other: The University of Pennsylvania Smell Identification Test (UPSIT)

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this study is to determine whether survivors of Legionnaires' disease suffer smell loss. A quantitative olfactory test will be performed by the participants. Such testing will require approximately 20-30 minutes of the participant's time. The participants will take the University of Pennsylvania Smell Identification Test (UPSIT), a scratch-and-sniff test to assess their ability to identify odors in a forced- choice format. Volunteers will also complete a questionnaire asking personal history, demographic questions, and medical history.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Persons of generally good health, as obtained from a screening questionnaire who are 18 years of age and older
  • Both men and women of all ethnic backgrounds will be accepted.

Exclusion criteria

  • Age less than 18
  • Pregnant Women
  • Persons who mental competence is limited, such as those with dementia

Trial design

10 participants in 2 patient groups

Legionnaires' Disease Volunteers
Description:
Volunteers who have been diagnosed/survivors of Legionnaire's Disease
Treatment:
Other: The University of Pennsylvania Smell Identification Test (UPSIT)
Healthy Volunteers
Description:
Volunteers who are healthy.
Treatment:
Other: The University of Pennsylvania Smell Identification Test (UPSIT)

Trial contacts and locations

1

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Central trial contact

Rafa Khan, BA; Richard L Doty, PhD

Data sourced from clinicaltrials.gov

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