Status:

RECRUITING

Safety and Performance Assessment of the Decongestant Seawater Spray Pocket Valve Enriched With Essential Oils in Patients With Acute Rhinitis Associated With Nasal Obstruction: "DEVALPO"

Lead Sponsor:

Laboratoires Gilbert

Collaborating Sponsors:

EVAMED

Conditions:

Acute Rhinitis

Nasal Obstruction

Eligibility:

All Genders

12+ years

Phase:

NA

Brief 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 ...

Eligibility Criteria

Inclusion

  • 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.

Exclusion

  • 1\. Pregnant and/or breastfeeding woman
  • 2\. Hypersensitivity to seawater and/or known allergies to any of the ingredients of the spray.
  • 3\. Diseases causing narrowing of the airways (e.g. asthma, chronic obstructive pulmonary disease (COPD)) and/or respiratory insufficiency.
  • 4\. Patients with uncontrolled asthma (GINA score greater than or equal to 4)
  • 5\. Patients undergoing allergy desensitization
  • 6\. Patients suffering from chronic nasal obstruction due to a deformation of the nasal wall or nasal polyps. creams or gels.
  • 7\. Patients taking local and systemic vasoconstrictors, corticosteroids, nonsteroidal anti-inflammatory drugs (NSAIDs), antibiotics, and local antiseptics.
  • 8\. Concomitant use of other nasal sprays, essential oils for local nasal use, creams, or gels for the nose.
  • 9\. Patients under guardianship, conservatorship, or legal protection.

Key Trial Info

Start Date :

June 23 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 30 2026

Estimated Enrollment :

101 Patients enrolled

Trial Details

Trial ID

NCT05494346

Start Date

June 23 2023

End Date

June 30 2026

Last Update

September 25 2025

Active Locations (5)

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Page 1 of 2 (5 locations)

1

Cabinet Médical

Blainville-sur-Orne, France, 14550

2

Cabinet Médical Caen

Caen, France, 14000

3

MSP du Haut Anjou

Châteauneuf-sur-Sarthe, France, 49330

4

Cabinet Médical Gainneville

Gainneville, France, 76700