Allergic Rhinitis Clinical Trials

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Prospective Multicenter Clinical Investigation Evaluating the Performance and Safety of Gilbert Laboratories' Decongestant Seawater Spray Pocket Valve Enriched With Essential Oils

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this pre-market clinical investigation is to assess the safety and the performance of decongestant seawater spray pocket valve enriched with essential oils by Gilbert Laboratories. The study will evaluate the results of acute rhinitis associated with nasal obstruction using the decongestant seawaterspray pocket valve enriched with essential oils over a 8 day period.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Healthy Volunteers: f
View:

• 1\. Patient ≥ 12 years.

• 2\. Patient with acute rhinitis associated with nasal obstruction during infectious episodes such as rhinopharyngitis (cold), rhinosinusitis, or during non-infectious episodes such as allergic rhinitis.

• 3\. a. Informed adult patient who has given written consent prior to any study specific procedure. b. Informed minor patient who has given assent and whose legal guardians have given written consent prior to any study-specific procedure.

• 4\. Patient able to meet the study requirements for monitoring, spray use, and questionnaire completion.

• 5\. Patient affiliated to a social security scheme.

Locations
Other Locations
France
Cabinet Médical
RECRUITING
Blainville-sur-orne
Cabinet Médical Caen
RECRUITING
Caen
MSP du Haut Anjou
RECRUITING
Châteauneuf-sur-sarthe
Cabinet Médical Gainneville
WITHDRAWN
Gainneville
ALYATEC
COMPLETED
Strasbourg
Contact Information
Primary
Carine BRUNEL
cbrunel@labogilbert.fr
+33 (0)1 45 39 50 21
Time Frame
Start Date: 2023-06-23
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 101
Treatments
Other: Arm A: Patients with peak nasal flow performed
This arm is made up of major patients. Nasal flow point measurements will be performed at D0 and D3.
No_intervention: Arm B: No peak nasal flow
This arm is made up of minor patients. Unlike arm A, nasal flow measurements will not be performed at D0 and D3.
Related Therapeutic Areas
Sponsors
Collaborators: EVAMED
Leads: Laboratoires Gilbert

This content was sourced from clinicaltrials.gov