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Efficacy of Puressentiel Protective Nasal Spray in Allergic Rhinitis (EPPNS)

Primary Purpose

Allergic Rhinitis Due to Grass Pollen, Allergic Inflammation

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Puressentiel protective nasal spray
Sponsored by
Puressentiel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Allergic Rhinitis Due to Grass Pollen

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with diagnostic of allergic rhinitis sensitized to grass pollen for more than one year with or without associated asthma

Exclusion Criteria:

  • patients sensitized to a perrianual allergen
  • patients with viral infection 4 weeks before inclusion
  • patients with severe non controlled asthma
  • patients with chronic sinusitis
  • pregnancy or breast feeding
  • patients with hypersensitivity to essential oil (eucalyptus radie)
  • epileptic patient
  • patients treated with nasal corticosteroid or anti-histamine

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    allergic rhinitis

    Arm Description

    Puressentiel protective nasal spray

    Outcomes

    Primary Outcome Measures

    Change in concentration of IL-13 in the nasal lavage will be assessed
    measurement by ELISA

    Secondary Outcome Measures

    Change in concentration of IL-5 in the nasal lavage will be assessed
    Measurement by ELISA
    Change in concentration of IL-4 in the nasal lavage will be assessed
    Measurement by ELISA
    Change in Nasal Inspiratory Peak Flow will be assessed
    Measurement with a peak flow meter
    Change in Allergic Rhinitis Control test (ARCT) will be assessed
    5 questions questionnaire score from 0 to 25 (0 worse score), 25 (best score)

    Full Information

    First Posted
    November 10, 2020
    Last Updated
    January 7, 2021
    Sponsor
    Puressentiel
    Collaborators
    Institut National de la Santé Et de la Recherche Médicale, France
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04700852
    Brief Title
    Efficacy of Puressentiel Protective Nasal Spray in Allergic Rhinitis
    Acronym
    EPPNS
    Official Title
    Efficacy of Puressentiel Protective Nasal Spray on Symptoms and Inflammation in Patients With in Allergic Rhinitis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 1, 2021 (Anticipated)
    Primary Completion Date
    July 31, 2021 (Anticipated)
    Study Completion Date
    September 30, 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Puressentiel
    Collaborators
    Institut National de la Santé Et de la Recherche Médicale, France

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study is a proof o concept aiming to determine the efficacy of Puressentiel nasal protective spray (PNPS) in patients with allergic rhinitis. Cross over study, with a nasal provocative test (NPT) in patients with allergic rhinitis sensitized to grass pollen. A day 0 (first NPT) the following outcomes are recorded: allergic Rhinitis control test (ARCT) and Inspiratory nasal peak flow (INPF) before and 30 min after the NPT. Nasal lavage is performed 30 min after the NPT and 3 cytokines (IL4, IL5 and IL13 are measured by ELISA. An other NPT is performed at day 30 and the same outcomes measured. 30 min before NPT 2 nasal sprays of PNPS are administered in each nostril in a randomized manner and cross over, the patient being is own control. The primary outcomes ins the IL4, IL5 and IL13 concentrations in the nasal lavage. ARCT and INPF are the secondary outcomes.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Allergic Rhinitis Due to Grass Pollen, Allergic Inflammation

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    15 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    allergic rhinitis
    Arm Type
    Experimental
    Arm Description
    Puressentiel protective nasal spray
    Intervention Type
    Device
    Intervention Name(s)
    Puressentiel protective nasal spray
    Intervention Description
    provocative nasal test with grass pollen and nasal lavage
    Primary Outcome Measure Information:
    Title
    Change in concentration of IL-13 in the nasal lavage will be assessed
    Description
    measurement by ELISA
    Time Frame
    measurements at day 1 and day 30
    Secondary Outcome Measure Information:
    Title
    Change in concentration of IL-5 in the nasal lavage will be assessed
    Description
    Measurement by ELISA
    Time Frame
    Day1 and Day30
    Title
    Change in concentration of IL-4 in the nasal lavage will be assessed
    Description
    Measurement by ELISA
    Time Frame
    Day1 and Day 30
    Title
    Change in Nasal Inspiratory Peak Flow will be assessed
    Description
    Measurement with a peak flow meter
    Time Frame
    Day 1 and Day 30
    Title
    Change in Allergic Rhinitis Control test (ARCT) will be assessed
    Description
    5 questions questionnaire score from 0 to 25 (0 worse score), 25 (best score)
    Time Frame
    Day 1 and day 2

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: patients with diagnostic of allergic rhinitis sensitized to grass pollen for more than one year with or without associated asthma Exclusion Criteria: patients sensitized to a perrianual allergen patients with viral infection 4 weeks before inclusion patients with severe non controlled asthma patients with chronic sinusitis pregnancy or breast feeding patients with hypersensitivity to essential oil (eucalyptus radie) epileptic patient patients treated with nasal corticosteroid or anti-histamine
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Davide Caimmi, MD
    Phone
    33630061134
    Email
    davide.caimmi@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Elisabeth Simon, PhD
    Phone
    33144405528
    Email
    e.simon@puressentiel.com

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Efficacy of Puressentiel Protective Nasal Spray in Allergic Rhinitis

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