RecruitingPhase 2ACTRN12606000095561

“Sleep disturbances in subjects with asthma and rhinitis”

" A double blind, randomised, placebo controlled, cross-over, intervention study evaluating the effect of treating rhinitis in asthma with intranasal steroids to improve sleep.


Sponsor

The Woolcock Institute

Enrollment

30 participants

Start Date

Mar 10, 2006

Study Type

Interventional

Conditions

Summary

A majority of patients with asthma has nasal inflammation but it is not always diagnosed and treated. Nasal inflammation cause sleep disturbances that can be improved by treatment with nasal steroid spray. It has not been studied before if treatment with nasal steroids can improve sleep in patients with asthma. We will investigate 30 patients with asthma to see if their "quality of sleep" and "quality of life" can be improved by treament with nasal steroid spray compared to placebo.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 50 Yearss

Exclusion Criteria1

  • Pre-existing treatment with nasal steroids which is not able to be stoppedKnown obstructive sleep apnoea syndrome (OSAS)Treatment with oral steroidsPrevious hospitalisation (within the last 12 months) for asthmaInhaled steroid dosage exceeding 1000µg/day (fluticasone) or 1600ug/day (budesonide)Treatment with sedativesTreatment with neuroleptic pharamceuticalsNasal polypsSevere septal deviation or turbinate hypertrophy.

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Interventions

6 weeks of intranasal Fluticasone spray 400 ug daily

6 weeks of intranasal Fluticasone spray 400 ug daily


Locations(1)

Australia

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ACTRN12606000095561