Chronic Rhinitis
Conditions
Keywords
Rhinitis
Brief summary
A randomized, sham-controlled, double-blind study of the NEUROMARKTM system as a treatment for chronic rhinitis
Detailed description
The MERIDIEN Study is a prospective, multi-center, double-blind, randomized (1:1), sham-controlled, cross-over study to evaluate the safety and efficacy of the NEUROMARK™ System in patients with Chronic Rhinitis.
Interventions
DEVICENEUROMARK™ System
The NEUROMARK™ System is designed to deliver energy to the nasal cavity intended to interrupt nasal nerves aimed to reduce symptoms related to Chronic Rhinitis.
DEVICESham Device
A Sham device will be used in the nasal cavity
Sponsors
Neurent Medical
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Masking description
Subjects, site investigator, site personnel, and sponsor will be blinded to which study arm they are randomized to.
Intervention model description
Randomized, Double-blind, Sham Controlled Study
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Subject provides written informed consent, including authorization to release health information. * Subject is 18 years of age or older at the time of consent. * Subject has provided a negative pregnancy test (if Subject is a woman of childbearing potential (WOCBP). * Subject WOCBP must be practicing and willing to continue an effective method of birth control during the course of the study. * Subjects stated willingness to comply with all study procedures, post- treatment care and availability for the duration of the study follow up of 1 year. * Subject tests negative for active COVID-19 at the start of study screening and continues to be free from COVID-19 symptoms until the time of enrollment/treatment. * Subject understands and agrees to follow local COVID-19 restrictions (social distancing, face mask, etc.)
Exclusion criteria
* Subject has an allergy or intolerance to anaesthetic agent or other study-required materials. * Subject is an active smoker or has been a smoker within the last 6 months (patient reported). * Any physical condition that in the Investigator's opinion would prevent adequate study participation or pose increased risk to the study Subject. * Subject is pregnant, nursing or plans to become pregnant during the study, or is a WOCBP, but is not willing to use an effective method of birth control. * Patient is enrolled in an investigational drug or device study or has participated in such a study within the last 30 days prior to screening that in the opinion of the Investigator would interfere with the study results * Patient presents with any condition or situation which, in the Investigator's opinion, puts the Subject at risk, could confound the study results, or may interfere significantly with the Subject's participation in the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Frequency of Serious Adverse Events (SAEs) directly attributable to the device | 1 month | Safety |
Countries
United States
Outcome results
None listed