CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 30 enrolled
Drug / intervention
Fluticasone Propionate_1.5 +3 moredrug
Likely dose
Fluticasone Propionate_1.5 50 microgramsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00692978
NCT00692978Phase 4Completed

The Pharmacokinetics of Inhaled Fluticasone Propionate Delivered as Monodisperse Aerosols

Imperial College London·interventional·Posted Jun 6, 2008·Updated Nov 25, 2020

In Brief

A Phase 4 clinical trial evaluating Fluticasone Propionate_1.5, Fluticasone Propionate_3, and 2 other interventions for Healthy and Asthma. Completed, enrolled 30 participants across 2 sites.

Detailed Summary

Asthma is most effectively treated by delivering inhaled drugs from an inhaler (puffer) directly into the lungs. Inhaled steroids are used in asthmatic patients to dampen down lung inflammation, which unchecked, can often lead to patient symptoms. Inhalers deliver a mist containing particles of lots of different sizes (like hairsprays). Medical puffers used by patients produce a 'coarse' mist of drug particles, which have the potential for side effects, as different sized particles will reach different parts of the airways and include; the mouth, the throat, the windpipe, and the bloodstream (all places we do not want the inhaled drug to go - and can give rise to important side effects)and, the lungs (where we do want the drug to 'deposit'). Our aim in this study is to test an inhaled steroid by giving it to subjects as a 'fine' mist containing drug particles of nearly all one size using a research nebuliser (a Spinning Top Aerosol Generator). We shall use small, intermediate and large drug particle mists. We aim to find out how much of the drug goes to the blood stream for each particle mist and compare it with the standard puffers used in routine clinical practice. We hope this study will provide information to the rationale that by improving the efficiency of drug delivery (by changing drug particle size) one may improve inhaled drug delivery and ultimately, clinical patient benefit. Healthy volunteers and asthmatic patients will be recruited at the Royal Brompton Hospital London. The study is funded by GlaxoSmithKline, Research \& Development, U.K.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy, Asthma
CountriesUnited Kingdom
Collaborators--

Timeline

Phase 4CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 6, 2008
Enrollment StartAug 1, 2008
Primary CompletionJul 3, 2011
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 18.1 years ago

Interventions

Fluticasone Propionate_1.5drug

Dose 50 micrograms (total dose), Monodisperse aerosol with particle size of drug 1.5 micros, inhaled

Fluticasone Propionate_3drug

Dose 50 micrograms (total dose), Monodisperse aerosol with particle size of drug 3.0 microns, inhaled

Fluticasone Propionate_6drug

Dose 50 micrograms (total dose), Monodisperse aerosol with particle size of drug 6.0 microns, inhaled

FP From Active 250 ug MDI Inhalerdrug

Monodisperse aerosols inhaled of Fluticasone Propionate at 250micrograms dose with active MDI inhaler