Clinical trials: Parosmia
Dysosmia, Anosmia
Treatment of Pediatric Patients That Lost Sense of Smell Due to COVID-19
This research study is a randomized controlled trial in pediatric and young adult patients who have lost their sense of smell due to COVID-19 viral infection. The goals are: 1.
- Conditions
- Dysosmia, Anosmia, Covid19
- Trial name
- NCT04964414
- Testing
- Smell Retraining, Budesonide
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Amanda Stapleton
Anesthesia, Pediatrics
Chocolate or Sevoflurane: Use of Parosmia to Facilitate More Cooperative Inhalation Inductions in Children
Children undergoing surgery and anesthesia are often negatively impacted by anxiety and fear in the preoperative period. Routine inhalational anesthetic induction is a unique aspect of pediatric anesthesia.
- Trial name
- NCT06449157
- Testing
- Inhalation induction with parosmia
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Johns Hopkins University
Parosmia, Smell Disorder
Triggers for Post-Viral Parosmia
Background: Many people lose their sense of smell after they have had a cold, flu or sinus infection. Recovery (if at all) generally starts with a "parosmia" phase which means every-day smells become distorted and over-poweringly…
- Trial name
- ParosmiaQ (NCT04868435)
- Where
- United Kingdom
- Volunteers
- 943 people
- Sponsor
- University of Reading
Anosmia, Covid19
COVID-19 Anosmia Study
To capture the natural history of COVID-19 associated olfactory dysfunction as measured by two patient reported outcome measures (SNOT-22, QOD-NS) and a 6-week BSIT with a comparison to an intervention arm receiving daily omega-3…
- Trial name
- NCT04495816
- Testing
- Omega-3 Fatty Acid Supplement
- Where
- United States
- Volunteers
- 139 people
- Sponsor
- Icahn School of Medicine at Mount Sinai
Paraosmia
Randomized Clinical Trial of Intranasal Injection of Platelet-Rich Plasma for Treatment of Parosmia
This randomized clinical trial will evaluate the benefit of platelet-rich plasma (PRP) in the treatment of qualitative olfactory dysfunction (parosmia).
- Trial name
- NCT06283745
- Testing
- Platelet-rich Plasma (PRP), Saline
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- Stanford University