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N/A N=51 Treatment

Steroid Nasal Irrigation for Flavor Evaluation and Detection Study

Olfactory Disorder

Enrolled (actual)
51
Serious AEs
0.0%
Results posted
Nov 2022
Primary outcome: Primary: Pre- and Post-intervention Difference in Functional Connectivity Before and After Smell Training. — 5 Regions of interest

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Smell training (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Washington University School of Medicine
Primary completion
Nov 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Pre- and Post-intervention Difference in Functional Connectivity Before and After Smell Training.
5
SECONDARY
Pre- and Post-intervention Difference in Smell Testing Before and After Budesonide Treatment
19.5; 17.5
SECONDARY
Subjective Response to Smell Training Intervention
23.8
SECONDARY
Comparison of Olfactory Network in Healthy Controls to Study Participants
13
SECONDARY
Pre- and Post-intervention Difference in Smell Testing Before and After Smell Training
19; 18.3
SECONDARY
Pre and Post Difference in QOD-NS After Smell Training
7.4

Summary

The purpose of this research study is to examine the efficacy of a 12-week smell training intervention for participants with olfactory dysfunction following an infection of the upper respiratory tract.

Eligibility Criteria

Inclusion Criteria

  • Age between 18 and 70
  • Anosmia or hyposmia (UPSIT <34 (male), UPSIT <34 (female); Sniffin' Sticks threshold below 5.5)

Exclusion Criteria

  • Inability to understand English
  • Current smoker or history of smoking within the past 6 months
  • Current nasal polyps
  • Exposure to head and or/neck radiation
  • Exposure to chemotherapy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02985515). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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