Olfactory Outcomes of Dupilumab Treatment for Nasal Polyposis

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorLondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

About this trial

The study aims to investigate the olfactory TDI score (Threshold, Discrimination, Identification) using the Sniffin' sticks test for patients with chronic rhinosinusitis with nasal polyps (CRSwNP) on dupilumab. Twenty-seven adult patients will be followed up during the treatment with dupilumab on three visits to the Otolaryngology Clinic (Baseline, 3 months and 6 months).

The primary endpoint will be the TDI score. Nasal polyp score, Quality of Olfactory Disorders - negative symptoms (QOD-NS symptom scores), SNOT-22 will be secondary endpoints.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients older than 18 years old

Chronic rhinosinusitis with Nasal Polyps

Olfactory loss

Clinical indication for treatment with Dupilumab

Disqualifiers

Sinonasal malignancies

Trauma

Idiopathic olfactory loss

Use of cocaine

Trial design

Design model

Single group

Treatments tested in this trial

  • Dupilumab 300 MG/2 ML Subcutaneous Solution [DUPIXENT]

    Drug

    Dupilumab will be administered subcutaneously for 6 months (1 initial 600mg dose + 5 300mg doses every 4 weeks)

Treatment groups

27 Participants
are divided into 1 treatment group
Group A: Dupilumab groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change from Baseline in the Smell Threshold, Identification and Discrimination (TDI score) at week 12 and week 24.

The Sniffin' Sticks test involves testing odor for threshold and discrimination whilst blind folded and secondly odor identification. The sum of four odors responses ranges from 0-16. The sum of total score from odor Threshold, Discrimination and Identification (TDI) is a maximum of 48 points. The total score is graded as; normosmia equals or over 30.5 points, hyposmia 16.5-30 points and anosmia less than 16.5 points.

Time frame
Baseline, 12 weeks and 24 weeks.

Secondary outcomes

1

Change from Baseline in the Nasal Polyps score at weeks 12 and 24.

Nasal Polyps score is the sum of the right and left nostril scores (endoscopic assessment). Total score ranges from 0 (no polyps) to 8 (large polyps on for each nostril \[4+4\] ).

Time frame
Baseline, 12 weeks and 24 weeks.
2

Change from Baseline in the Sino-nasal outcome test- 22 (SNOT-22) at weeks 12 and 24.

SNOT-22 is a validated questionnaire to assess the impact of chronic rhinosinusitis on patients' quality of life. Patient grades the impact of 22 potential symptoms in their life, by choosing from 0 \[no problem\] to 5 \[problem as bad as it can be\]. Highest possible score is 10 (worst quality of life); minimal clinically important change ≥ 8.90

Time frame
Baseline, 12 weeks and 24 weeks.
3

Change from Baseline in the QOD-NS at weeks 12 and 24.

Quality of Olfactory Disorders - negative symptoms (questionnaire)

Time frame
Baseline, 12 weeks and 24 weeks.

Other outcomes

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