CClinicalTrials.gg
TerminatedNCT03364959MASQUEUpdated Jun 7, 2024

Ex Vivo Pilot Study of the Impact of Nasal Breathing During the Administration of Inhaled Corticosteroids by Inhalation Chamber in Asthmatic Children Ages Between 1 and 4-year-old

An interventional study of Corticosteroids inhalation and Corticosteroids inhalation in Asthma in Children, sponsored by Assistance Publique Hopitaux De Marseille. Terminated at 1 site in France. Open to participants aged 1 Year to 4 Years. Per ClinicalTrials.gov, last updated 2024-06-07.

Sponsored by Assistance Publique Hopitaux De Marseille · Not applicable, Interventional, and Treatment

Why this study was terminated
lack of inclusion
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
1 Year to 4 Years
Sex
All
01

Study summary

The main purpose of this open randomized, ex-vivo comparative study, is to assess and to compare the inhalable dose of inhaled corticosteroid collected through a nasal filter and a mouth filter located in a partitioned face mask and delivered to an infant with asthma via a Tipshaler® holding chamber

Read the detailed description

The use of a face mask is recommended for inhaled treatments delivered from a pressurized metered-dose inhaler and a spacer device in infants and young children with respiratory disorders such as asthma.

The nose effectively filters the air particles and it may reduce the amount of inhaled drug. Thus it is reported that the drug deposited in the lung dose is halved in older children inhaling through the nose with respect to those inhaling through the mouth.

In very young children the efficiency of nasal filtration is unknown for inhaled treatment. In infants, an in-vitro study suggests that nasal breathing allows a similar or more important drug delivery than mouth breathing, contrary to what is observed in the oldest and adults.

So it seems of great import to characterize the drug delivery in this age group comparing the nasal with the mouth breathing.

The main purpose of this open randomized, ex-vivo comparative study, is to assess and to compare the inhalable dose of inhaled corticosteroid collected through a nasal filter and a mouth filter located in a partitioned face mask and delivered to an infant with asthma via a Tipshaler® holding chamber. 60 children, aged between 1 and 4 years old, with a medically diagnosed asthma will be recruited. Each child will inhale four puffs of both Fluticasone 125 µg/puff and Beclometasone dipropionate 100 µg/puff administered by a single observer in a standardized and randomized way. No drug will be inhaled by the children. The drugs collected on the filters between the holding chamber and patient will be analysed by high performance liquid chromatography HPLC). Filter doses will be expressed in percentage of the total dose filtered. The analysis will cover the difference between oral dose and nasal dose compared to zero. Student's test will be performed with p \< 0.05.

02

Conditions studied

  • Asthma in Children
03

Who can participate

Ages eligible
1 Year to 4 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Aged from 1 to 4 years old
  • Male or female
  • With medically diagnosed asthma
  • Patients who are used to use an inhalation chamber with a face mask
  • Patients who have not had asthmatic decompensation for at least 1 month.
  • Patients' parents having given their written consent
  • With normal clinical respiratory examination on the day of the test.

Exclusion criteria

Exclusion Criteria:

  • Patients whose parents are unable to understand the purpose and conditions of the study
  • Patients whose parents are unable to give their consent
  • Patients participating in another clinical trial or exclusion period from a previous clinical trial
  • Patients presenting with a nasopharyngeal infection in the previous month
  • Child with nasal obstruction, nocturnal snoring, adenoid facies or facial malformation
  • Patient presenting with an asthmatic decompensation episode in the previous month
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Flixotide

    Patients inhale first Flixotide and then Qvar

    Other: Corticosteroids inhalation

  • Experimental
    Qvar

    Patients inhale first Qvar and then Flixotide

    Other: Corticosteroids inhalation

Interventions

  • OtherCorticosteroids inhalation

    Flixotide inhalation followed by Qvar inhalation through a nasal filter and a mouth filter located in a partitioned face mask and delivered to an infant with asthma via a Tipshaler® holding chamber

  • OtherCorticosteroids inhalation

    Qvar inhalation followed by Flixotide inhalation through a nasal filter and a mouth filter located in a partitioned face mask and delivered to an infant with asthma via a Tipshaler® holding chamber

05

What researchers measure

Primary outcomes

  1. Percentage (%) of corticoisteroids proportion delivered to the nose with respect to the mouth by chromatography.

    Compare by chromatography the proportion of product administered to the nose with respect to the mouth for the administration of inhaled corticosteroids in children with asthma. Filter doses will be expressed as a percentage of the total filtered dose.

    Time frame: 12 months

06

Study locations

1 site
  • Assistance Publique Hopitaux de Marseille
    Marseille, 13354, France
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03364959
Lead sponsor
Assistance Publique Hopitaux De Marseille
Responsible party
Sponsor
First posted
Dec 7, 2017
Start date
Oct 23, 2018
Primary completion
Oct 10, 2019
Completion
Jul 9, 2021
Last update
Jun 7, 2024

Study contacts

Jean-Olivier ARNAUD, Director
study director · Assistance Publique Hôpitaux de Marseille

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion