Completed
JawRhin1Sleep Respiratory Disorders in Patients With Moderate to Severe Persistent Rhinitis: a Prospective, Predictive Study
What is being collected
Data Collection
Collected at a single point in time - Cross-sectionalWho is being recruted
Infections+3
+ Nose Diseases
+ Otorhinolaryngologic Diseases
Over 18 Years
+12 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: January 2020
Summary
Principal SponsorUniversity Hospital, Montpellier
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner
Study start date: January 28, 2020
Actual date on which the first participant was enrolled.The secondary objectives of the study are to evaluate the concordance and correlation between: * MM-RDI, * the respiratory effort evaluated by MM, * polysomnography (PSG) results, * quality of life questionnaires, * clinical data, * treatments.
Official TitleSleep Respiratory Disorders in Patients With Moderate to Severe Persistent Rhinitis: a Prospective, Predictive Study
Principal SponsorUniversity Hospital, Montpellier
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
55 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
InfectionsNose DiseasesOtorhinolaryngologic DiseasesRespiratory Tract DiseasesRespiratory Tract InfectionsRhinitis
Criteria
4 inclusion criteria required to participate
Patient consulting for persistant, moderate-to-severe rhinitis
The patient has signed the informed consent
The patient is a beneficiary of a social security programme (national health insurance)
Patient living in the Montpellier region (< 30 kilometers).
8 exclusion criteria prevent from participating
The patient is in an exclusion period determined by another study
It is impossible to correctly inform the patient
The patient is participating in another study that precludes participation in the present study
The patient cannot fluently read French
Show More Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Suspended
CompletedOne Study Center