Terminé

The Clinical Effect in Asthma of Inhaled Fluticasone Propionate Delivered as Monodisperse Aerosols

0 critères remplis à partir de votre profilVoyez en un coup d'œil comment votre profil répond à chaque critère d'éligibilité.
Ce qui est testé

1.5 microns at 50mg

+ 6 microns at 50mg

+ Placebo Comparator

Médicament
Qui peut participer

Maladies bronchiques+6

+ Hypersensibilité

+ Hypersensibilité immédiate

De 18 à 65 ans
+16 critères d'éligibilité
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Étude thérapeutique

Groupe PlaceboPhase 4
Interventionnel
Date de début : décembre 2011
Voir le détail du protocole

Résumé

Sponsor principalImperial College London
Dernière mise à jour : 18 novembre 2019
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Date de début de l'étude : 1 décembre 2011

Date à laquelle le premier participant a commencé l'étude.

Inhaled drug therapy is an established and effective means to treat lung diseases such as asthma. Medical inhalers ('puffers') form the cornerstone of the management of patients with respiratory/lung problems. Inhaled treatment usually comprises placing an inhaler (puffer) in the mouth and inhaling a measured dose of drug from the puffer. The drug dose needs to bypass the throat and reach the lungs, in order to be effective. However, there is still much that is not known about what actually happens to the inhaled drug in the lungs. Much of the inhaled drug dose from a puffer fails to reach the lungs with most of it hitting the back of the throat. Only a small amount (approximately as little as 20%) of the drug reaches the important parts of the lungs to have a beneficial effect. Particle size has a significant influence on our ability to get the inhaled drug to the important parts of the lungs. In order to get the inhaled drug to these important parts of the lungs it is necessary to understand how much of a clinical improvement is obtained when identical doses of FP are inhaled with different particle sizes. Inhalers (are a bit like hairspray cans or air fresher cans) and produce aerosol clouds of particles. Medical inhalers come in different shapes and sizes and have a variety of drugs used to treat patients. Inhalers used in routine clinical practice produce a 'coarse' mist of drug particles, which have the potential for side effects, as different sized particle will deposit in different parts of the respiratory tract and include; the mouth, the throat, the windpipe, and the bloodstream (all places we do not want the inhaled drug to 'deposit') and the lungs (where we do want the drug to go). This is particularly an important consideration with inhaled steroids that are commonly used in the management of patients with asthma and bronchitis and emphysema. For example, a common side effect is that the deposition of steroid drug in the throat can lead to a hoarse or altered voice, and sometimes thrush of the throat. In contrast, monodisperse aerosols are special 'fine-mist' aerosols, where all the drug particles are of one particle size. We can use these aerosols to investigate the science of the way the lungs handle and respond to inhaled drugs of different particle size. We shall use small and large drug particles. In order to deliver the inhaled drug as a monodisperse aerosol, we shall use a spinning top aerosol generator (STAG) (a large research nebuliser machine) which is able to selectively generate aerosol clouds that have a fine mist. This is an efficient machine compared to current nebulisers used in routine clinical practice, where it can often be difficult to control the inhaled drug dose to the patient; sometimes the patient gets too little a dose because the nebuliser is an inefficient inhaler device. But, also, by improving the efficiency of inhaled drug delivery - will allow lower drug doses to be used - which will decrease the potential for patient side effects. We have previously undertaken and published in the medical literature a series of clinical studies in patients with asthma using the STAG 'fine-mist' aerosol system and the 'reliever' drug salbutamol (ventolin). Also, we are currently undertaking the investigation of the pharmacokinetic effects of inhaling the 'preventer ' steroid class of drug FP at different particle sizes. The main question is now can we improve the beneficial effect the inhaled drug has on the lungs by altering the particle size. This study will form the next step in the investigation of this commonly used inhaled steroid Fluticasone Propionate, used in asthma, bronchitis and emphysema patients. We hope this investigation will help to provide further answers to the rationale that by improving the efficiency of drug delivery (by changing drug particle size) one may improve inhaled drug delivery and improve clinical benefit.

Sponsor principalImperial College London
Dernière mise à jour : 18 novembre 2019
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

21 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Traitement

Cette étude teste un ou plusieurs traitements pour évaluer leur efficacité contre une maladie ou un problème de santé spécifique. L'objectif est de voir si un nouveau médicament ou une thérapie fonctionne mieux, ou provoque moins d'effets secondaires que les options existantes.



Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

De 18 à 65 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains non autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Maladies bronchiquesHypersensibilitéHypersensibilité immédiateMaladies du Système ImmunitaireMaladies pulmonairesMaladies pulmonaires obstructivesHypersensibilité respiratoireMaladies des voies respiratoiresAsthme

Critères

5 critères d'inclusion nécessaires pour participer
Asthmatic patients who are free from significant cardiac, gastrointestinal, hepatic, renal, haematological, neurological and psychiatric disease

Male or females aged greater than 18 years with a documented history of reversible airways disease responding to beta2-adrenergic therapy

Not taking any regular medication that is contraindicated in those about to receive fluitcasone propionate (as indicated in the British National Formularly); other than the oral contraceptive pill

Patients who are able and willing to give written informed consent to take part in the study

Voir plus de critères

11 critères d'exclusion empêchent la participation
Any female volunteer or females who are pregnant or lactating or are likely to become pregnant during the trial. Women of child-bearing potential may be included in the study if, in the opinion of the investigator, they are taking adequate contraceptive precautions

Any patient with a contraindication to taking an inhaled steroid and specifically FP, listed in the British National Formulary will not be entered into this study

Participants with a known or suspected allergy to corticosteroids or any component of the formulations and/or Suspected hypersensitivity to inhaled corticosteroid (this will be asked directly at the screening visit)

Subjects that have received inhaled or intravenous fluticasone propionate in the last 2 months

Voir plus de critères

Plan de l'étude

Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.
Groupes de traitement
Objectifs de l'étude

4 groupes d'intervention sont désignés dans cette étude

25% de chances d'être dans le groupe placebo en aveugle

Groupes de traitement

Groupe I

Comparateur actif
50 mg of monodisperse Fluticasone Propionate delivered as 1.5 microns aerosol followed by AMP PC20 challenge test

Groupe II

Comparateur actif
50 mg of monodisperse Fluticasone Propionate delivered as 6.0 microns aerosol followed by AMP PC20 challenge test

Groupe III

Placebo
No active drug, just solvent delivered from STAG followed by AMP PC20 challenge test

Groupe IV

Comparateur actif
Fluticasone Propionate , Metered dose inhaler, 250 mg dose followed by AMP PC20 challenge test

Objectifs de l'étude

Objectifs principaux

Objectifs secondaires

Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.

Cette étude comporte 2 sites

Asthma Lab, Royal Brompton Hospital

London, United KingdomOuvrir Asthma Lab, Royal Brompton Hospital dans Google Maps

Department of Nuclear Medicine, Royal Brompton Hospital

London, United Kingdom
Terminé2 Centres d'Étude