Olfactory Training on Smell Dysfunction Patients in HK

Pamela Youde Nethersole Eastern Hospital

Status: Enrolling

Conditions: Olfaction Disorders; Smell Dysfunction; Anosmia; Smell Loss; Hyposmia; Olfactory Impairment; Smell Disorders

Treatments: Other: Olfactory Training; Other: Control

Study type: Interventional

Funder types: Other

Identifiers

NCT05364125

OlfactoryTrainingHKRCT

Details and patient eligibility

About

• Causes of olfactory dysfunction can be classified into conductive and sensorineural causes.
• Conductive causes are mainly due to structural nasal problem, which can be treated by nasal surgery
• Sensorineural causes included post-infection, post-head injury, post Head and Neck irradiation and other central nervous system diseases.
• Olfactory Training is well established treatment for sensorineural olfactory dysfunction in foreign countries.
• Olfactory Training by neurological chemosensory stimulation using aromatic substances delivered via electronic portable aromatic rehabilitation (EPAR) diffuser was proved to be effective treatment in COVID-19 related olfactory dysfunction in recent Hong Kong study.
• However, there is a lack of local study on the effect of Olfactory Training in other non-COVID-19 sensorineural causes of olfactory dysfunction in Hong Kong population.

Full description

Design Prospective double-blinded randomized control trial.

Study Period 1/7/2022 - 30/6/2024 for case recruitment.

Suitable patient will be recruited. Informed consent will be signed. Objective smell assessment will be done using the University of Pennsylvania Smell Identification Test (UPSIT) and Butanol Threshold Test (BTT). Subjective quality of life score will be obtained by Sino-Nasal Outcome Test (SNOT-22). Subjective smell and taste assessment will be assessed by Visual Analogue Scale (VAS). Patient will be randomized into treatment group and control group using computer generated list by an independent nursing staff. Doctors and the patients will be blinded during the study.

Enrollment: 80 estimated patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Olfactory dysfunction > 6 months and < 5 years

Exclusion criteria

• History of significant head injury (fracture, ICH)
• History of brain surgery
• History of nasal surgery
• Active nasal disease
• Active neurological disease
• Poor premorbid status/ non-communicable patients
• Mentally incompetent patients
• <18 years' old
• Pregnancy
• Hypersensitivity to the aromatic substance.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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80 participants in 2 patient groups, including a placebo group

Treatment arm

Experimental group

Description:

Olfactory training by neurological chemosensory stimulation using aromatic substances delivered via diffusers. Four aromatic substances will be used. Each substance will be given for 20 seconds sequentially, providing a total of 80 seconds of olfactory stimulation three times per day for 3 months.

Treatment:

Other: Olfactory Training

Control arm

Placebo Comparator group

Description:

Same diffuser will be given to control group. All of the four essential oils will be replaced by normal saline using the same packing. Same treatment regime of 20 seconds for each diffuser three times per day for 3 months will be instructed to control group patients.

Treatment:

Other: Control