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OpenTrials
Completed

NCT Number: NCT00559689

Study of Inhaled Glucocorticosteroid Administration in Asthma Patients

Once-daily inhaled glucocorticosteroids treatment can sufficiently control airway inflammation in asthma patients.

Completed

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hamamatsu University School of Medicine

Hamamatsu, 431-3192, Japan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Receive ICS for one year or more, with no change in dose within the previous 8 weeks

Exclusion criteria

  • Two or more courses of oral corticosteroid in the previous 12 months
  • Admission to hospital due to asthma in the previous 6 months
  • Admission to the intensive care unit due to asthma at any time in the past
  • Current cigarette smoker.

Treatment and study plan

Budesonide,hydrofluoroalkane-beclomethasone dipropionate

Drug

receive twice-daily administration

Budesonide,hydrofluoroalkane-beclomethasone

Drug

once-daily administration at bedtime

Primary outcomes

  1. once-daily administration of inhaled glucocorticosteroids can control airway inflammation

    Time frame: two-year

Sponsors and collaborators

Lead sponsor

Hamamatsu University

Other

Registry information

Official study title

Phase 4 Study of Once-Daily Inhaled Glucocorticosteroid Administration in Asthma Patients

Important dates

Study start
2005
Study completion
2007
First posted
Nov 16, 2007
Registry last updated
Mar 16, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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