Clinical Trial to Evaluate the Symptoms in Symptomatic Contact Lens Wearers Following Application of Intranasal Tear Neurostimulator Versus Control

A person is eligible for inclusion if he/she * In at least one eye, has a cotton swab nasal stimulation Schirmer test score at least 4 mm greater than 3 minute Schirmer with anesthesia basal score in the same eye at the Screening Visit * Is an adapted soft contact lens wearer and currently wears lenses an average of at least 2 days per week, with an average minimum wearing time of 3 hours each day over the past month and is able and willing to wear lenses for at least 6 hours on four study day visits * Has at least 20/40 visual acuity in both eyes with CL correction * Is symptomatic according to Young's categorization

* Refractive error surgery * Chronic or recurrent epistaxis, coagulation disorders or other conditions that may increase the risk of bleeding * History of nasal or sinus surgery * Vascularized polyp, deviated septum or severe nasal airway obstruction at the Screening visit * Cardiac demand pacemaker, implanted defibrillator, or other active implanted metallic or active implanted electronic device in the head