Elaboration of Patient-friendly Treatment Strategy With Capsaicin Nasal Spray in Patients With Idiopathic Rhinitis

Universitaire Ziekenhuizen KU Leuven

Status and phase

Completed

Phase 4

Conditions

Non-allergic Rhinitis

Treatments

Drug: Capsaicin

Drug: placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT02288156

TBM

Details and patient eligibility

About

Chronic rhinitis is affecting more than 200 million people worldwide. Its prevalence is estimated to be as high as 30% of the Western population. Rhinitis is defined as symptomatic inflammation of the inner lining of the nose and is characterized by the following symptoms: rhinorrhea, nasal blockage, nasal itching and/or sneezing. The cut-off point for defining rhinitis as chronic rhinitis is considered to be persisting symptoms for over more than twelve weeks Chronic rhinitis can be divided into three major subgroups; based on the knowledge of the major etiological factor: infectious rhinitis, allergic rhinitis and non-allergic, non-infectious rhinitis, in literature also referred to as nonallergic rhinitis. Non-inferiority in efficacy of the two novel treatment regimes i.e. capsaicin nasal spray 0,01mM (2puffs/nostril/day) during 4 weeks and capsaicin nasal spray 0,001mM (2puffs/nostril/day) during 4 weeks compared to the current treatment of capsaicin nasal spray 0,1mM (5/day administered on a single day) with regard to the change from baseline in VAS for major nasal symptom on week 4.

(Estimated placebo effect is 25%.)

Enrollment

80 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

idiopathic rhinitis patients with at least 2 persistent (> 12w) rhinological symptoms (nasal discharge, sneezing, nasal congestion) for an average of at least 1 h per day,
idiopathic rhinitis patients with a total nasal symptoms score (TNS) of 5 or more on a visual analogue scale (VAS).
Age > 18 and < 65 years.
Written informed consent.
Willingness to adhere to visit schedules.
Adequate contraceptive precautions in female patients with childbearing potential.

Exclusion criteria

Patients with concomitant allergic rhinitis, demonstrated by positive skin prick test (Hal reagents) and/or immunoglobins E in blood. *
Patients with structural abnormalities: nasal polyps, severe septal deviation (septum reaching concha inferior or lateral nasal wall), septal perforation, hypertrophy of the inferior turbinates.
Patients with local allergic rhinitis (LAR) or entopy.
Systemic steroid treatment less than 4 weeks before the inclusion in the study, nasal steroid spray less than 4 weeks before the inclusion, oral leukotriene antagonists or long-acting antihistamines less than 2 weeks before the inclusion.
Inability of the patient to stop taking medication affecting nasal function like ß-blockers.
History of prolonged use or abuse of decongestant nasal spray like xylometazoline spray and/or use or abuse of decongestive oral medication.
Evidence of infectious rhinitis/rhinosinusitis or common cold within 4 weeks prior to inclusion.
Pregnancy or lactation. **
Any disorder of which might compromise the ability of a patient to give truly informed consent for participation in this study.
Enrollment in other investigational drug trial(s) or receiving other investigational agent(s) for any other medical condition.
Contra-indications for the use of local anesthesia (cocaine 5%).
Smoking or occupational exposure to irritants (like hypochlorite, persulfates, isocyanates).
Nasal malignancies or severe comorbidity like granulomatosis or vasculitis.