Design of a Model to Study Functionality of the Trigeminal Nerve in Relation to Controlled Nasal Fractures
Design of a Model to Study Functionality of the Trigeminal Nerve in Relation to Controlled Nasal Fractures
The primary aim of the study is to create a model; in order to examine the effects of neural trauma in patients that are healthy individuals, induced by controlled nasal fractures during rhinoplasty, and the regeneration process in the weeks/months that follow. This study includes monitoring of subjective nasal symptoms with a visual analogue scale (VAS) score, peak nasal inspiratory flow (PNIF) measurements, collection of nasal secretions and nasal provocation (response to capsaicin and cold dry air (CDA) exposure).
The investigators will set up a prospective mono-center study. The investigators will utilize objective and subjective parameters in order to assess trigeminal nerve function at the level of the nasal mucosa before and after septorhinoplasty (as a model of controlled nasal fractures). The subjective parameters involve a visual analogue scale (VAS) score for each individual nasal symptom (nasal obstruction, facial pain/pressure, headache, rhinorrhea, sneezing, pruritus, post nasal drip, and loss of smell). An objective assessment includes measurement of PNIF (Peak Nasal Inspiratory Flow), the presence of neuropeptides in nasal secretions, (by introducing merocels and removing them 5 minutes later), short cold dry air (CDA) provocation and capsaicin provocation with subsequent measurements of PNIF and VAS scores and neuropeptides.
Inclusion Criteria:
Exclusion Criteria:
Age < 18 and > 65 years
Patients with nasal symptoms at baseline, defined as having more than 2,5 on VAS score
for individual nasal symptoms related to mucosal pathology
Nasal endoscopic signs of inflammatory pathology (rhinitis, rhinosinusitis with/without
nasal polyps)
Use of systemic steroid treatment, intranasal steroid treatment, oral leukotriene antagonists
or long acting antihistamines?
Asthma
Pregnancy or breastfeeding
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 is receiving other investigational
agent(s) for any other medical condition.
Contra-indications for local anaesthesia (Cocaine 5%)
Smoking
Systemic disease with lesions in ENT domain
Malignancies or severe comorbidity