Phase 2
N=77
Smell in COVID-19 and Efficacy of Nasal Theophylline (SCENT 3)
COVID-19
Bottom Line
View on ClinicalTrials.gov: NCT05947643 ↗Enrolled (actual)
77
Serious AEs
0.0%
Results posted
Aug 2025
Primary outcome: Primary: Clinical Global Impression - Improvement Scale — 9; 9 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- theophylline (Drug); Placebo (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Washington University School of Medicine
- Primary completion
- Apr 2025
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Clinical Global Impression - Improvement Scale |
9; 9 | — |
| SECONDARY Olfactory Dysfunction Outcomes Rating |
43.38; 45.96; 43.94; 45.26 | — |
| SECONDARY Assessment of Adherence |
1; 1; 1; 0; 1; 1 | — |
| SECONDARY Assessment of Blind |
20; 26 | — |
| SECONDARY Adverse Effects |
1; 0; 1; 0; 1; 0 | — |
Summary
The purpose of this Phase II trial is to test the effectiveness of intranasal theophylline irrigations for the treatment of COVID-19 related smell dysfunction. The investigators will compare the effect of theophylline nasal rinses versus placebo nasal rinses on smell symptoms. Participants will be asked to rinse their nose with a medication or placebo capsule dissolved in saltwater twice daily for 12 weeks and fill out surveys about smell before, during, and at the end of treatment.
This study will also be used to describe adverse effects related to intranasal theophylline irrigation.
Eligibility Criteria
Inclusion Criteria
- Participants will be recruited based on the following inclusion criteria:
- males and females ages 18 to 75 years
- located within or willing to travel to the state of Missouri or Illinois
- Olfactory dysfunction that has persisted for >3 months following suspected COVID-19 infection
- Baseline University of Pennsylvania Smell Identification Test (UPSIT) consistent with decreased olfactory function (<= 34 in women, <=33 in men). This test is a clinically validated 40-question forced-choice odor identification test where microencapsulated odorants on a strip are released by scratching.70 This will determine that patients have both subjectively and objectively diagnosed OD prior to undergoing treatment.
- Ability to read, write, and understand English and have access to email.
Exclusion Criteria
- Individuals will not be allowed to participate in this study if they meet one or more of the following exclusion criteria:
- History of olfactory dysfunction prior to COVID-19 infection
- Any use of concomitant therapies specifically for the treatment of olfactory dysfunction
- Use of or participation in previous trials of intranasal theophylline.
- Known existence of nasal polyps, prior sinonasal, or anterior skull-based surgery
- Dependence on theophylline for comorbid conditions such as asthma and chronic obstructive pulmonary disease (COPD)
- History of an allergic reaction to theophylline or other methylxanthines
- History of neurodegenerative disease (ie. Alzheimer's dementia, Parkinson's disease, Lewy body dementia, frontotemporal dementia)
- Pregnant or breastfeeding mothers.
- Current use of medications with significant (≥40%) interactions with theophylline, which include cimetidine, ciprofloxacin, disulfiram, enoxacin, fluvoxamine, interferon- alpha, lithium, mexiletine, phenytoin, propafenone, propranolol, tacrine, thiabendazole, ticlopidine, and troleandomycin.
Data sourced from ClinicalTrials.gov (NCT05947643). 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.