Intranasal Retinoic Acid Treatment for Patients With OlfactoryLOSS: A RANDOMIZED CONTROLLED TRIAL

Description

1. Purpose

To determine if there is an improvement in olfactory function following the use of intranasal Vitamin A in patients with post-inflammatory and/or post-traumatic olfactory loss.

2. Hypothesis

There a significant improvement in olfactory function in patients with olfactory loss using intranasal vitamin A when compared with patients with olfactory loss not using intranasal vitamin A

Null Hypothesis There is no significant improvement in olfactory function in patients with olfactory loss using intranasal vitamin A when compared with patients with olfactory loss not using intranasal vitamin A

3. Justification

To treat post inflammatory and post-traumatic olfactory loss, a few controlled studies have shown a positive effect of a specific therapy for olfactory loss, such as olfactory training (using repeated intensive stimulation of the olfactory system and the use of prednisone. Other drugs studied like Vitamin B and Zinc, have either been insufficiently studied or showed no significant effect on olfactory loss.

The use of Retinoic acid (Vitamin A), a fat-soluble vitamin, in the treatment of olfactory loss has been previously studied in both animal and human models and showed promise. However, no study has examined the use of topical administration of vitamin A. This study will be the first to examine this effect.

4. Objectives

Primary Objective To determine if there is an improvement in olfactory function following the use of intranasal Vitamin A in patients with post-inflammatory and/or post-traumatic olfactory loss.

Secondary Objectives To determine if patient quality of life is improved/affected by the use of intranasal vitamin A.

5. Research Method This is a Single blind Randomized Control Trial.

Procedure

The study population will be consecutive patients diagnosed with loss of olfactory function. It will be a single blind randomized control trial. Allocation concealment will be ensured by the use of sequentially numbered, opaque, sealed envelopes. An assessor blinded to which patient is using vitamin A will assess the primary outcome.

Consent will be obtained for this study following diagnosis of the patient. After diagnosis, the patient will be sent a consent form and will be recruited on the next clinic visit.

Screening: After diagnosis, there will be a screening period; inclusion/exclusion criteria for the study participation will be checked. Subjects who satisfy these criteria will be invited to participate in the study. The consent forms will be sent to them via email and their consent will be recorded.

Blinding: The study will be single-blinded study. The patients will be randomized into 3 arms/groups. An assessor blinded to which patient is using vitamin A will assess the primary outcome.

Study Arms/Groups: The patients will be randomized into 3 groups using the sealed envelope method. Each patient will be his or her own control. There will be two possible scenarios resulting from randomization:

• Group A: This study group will receive intranasal vitamin A at 10,000 I.U. per day and olfactory retraining using scented oils. Olfactory retraining is a validated and effective method of improving olfaction in patients with olfactory loss and is currently being used at our centre as standard of care. It involves smelling 4 scented oils for 40 minutes everyday for the duration of the study. This is performed by the patients. They will also receive their standard of care budesonide (Pulmicort) for their sinonasal disease. The Vitamin A will be mixed with the budesonide and applied using the mucosal atomization device (MAD). This is a device used to apply intranasal medication. It reduces the medication to tiny droplets so they can reach all parts of the nose and sinuses.
• Group B: This study group will receive Vitamin A and budesonide only. They will not receive olfactory retraining. These will also be applied using the MAD
• Group C: This study group will receive only standard of care budesonide. The medication will also be applied using the MAD.

Patients will also continue to receive all other standard of care medication and procedures as necessary.

6. Statistical Analysis

Sample size calculations According to the study conducted by Hummel et al, a the mean olfactory test (TDI) score was 19 with a standard deviation of 6.4. In order to have an 80% chance of detecting a clinically significant 6 point improvement in olfactory test (TDI) scores at a significant level of 5%, 108 patients will be required. This will be 36 patients per group. There is an approximately 10% drop out rate in studies conducted at the St Paul's sinus centre. Accounting for this drop out rate, a total of 120 participants (40 participants per group) will be required to conduct the study.

Statistical Comparisons Descriptive analysis will be used to describe demographic and some clinical outcomes. Mean, median and standard deviations will be used to describe these outcomes. The primary objective of this study is to compare olfactory function before and after the respective interventions among participants in the three groups. The dichotomous and continuous outcomes will be analyzed using Pearson Chi-squared test and analysis of variance (ANOVA). Analysis of variance will also be used to compare the olfactory test scores between the 3 groups and paired t-test for evaluating for statistical within the groups. Probability values less than 5% (=0.05) will be considered significant. Sub-analysis by etiology of olfactory loss will also be done using the same methods.

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