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Completed

NCT Number: NCT00614874

The Use of Rosiglitazone to Treat Asthma

Asthma is a common chronic disease characterized by airway inflammation and bronchoconstriction. This study utilizes the drug rosiglitazone (Avandia)to treat the effects of airway inflammation in patients with asthma.

The study will be conducted on 14 adult steroid naive patients with asthma. Patients with qualifying pulmonary function testing values will be eligible for enrollment. Enrolled subjects will be treated with rosiglitazone orally at 2mg dose for 4 weeks. Patients will be reassessed and dosing will increase in 4 week increments up to 8mg.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Creighton University Medical Center, Department of Pulmonology and Critical Care

Omaha, Nebraska, 68131, United States

About this study

The current standard-of-care utilizes corticosteroids to down-regulate the inflammatory state in patients with asthma. However, corticosteroids have many side effects and are not universally effective. New safe anti-inflammatory agents are needed to help modulate the disease. Peroxisome proliferator-activated receptor agonists are widely used to manage diabetes mellitus, another common chronic disease. These agents have been study models and have been shown to have anti-inflammatory effects in lung tissue. Case reports have noted improvement in asthma symptoms in patients being treated with these agents. These agents are ideally placed for human research given their long record of safe use in the treatment of type 2 diabetes.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Able to comprehend and grant a witnessed, written informed consent
  • Must be greater than 19 years old
  • Must be able to swallow a tablet
  • Female participants must have a negative urine pregnancy test at visit 1 and throughout duration of the study
  • Must have a history of physician diagnosed asthma
  • Must have a baseline FEV1 >60% predicted
  • Must be able to perform pulmonary function testing
  • Must have methacholine-induced decrease in FEV1 of 20%
  • Must be capable of withholding medications that may affect the methacholine challenge test
  • Must be able to withstand a 30 day washout period for all inhaled corticosteroids
  • Must be able to attend all office visits, 4 weeks apart for 12 weeks. Each visit will last approximately 2-3 hours

Exclusion criteria

  • Age 18 or younger
  • FEV1 <60% predicted value
  • History or presence of significant renal, hepatic,neurologic, cardiovascular, hematologic, cerebrovascular, respiratory, endocrine, gastrointestinal, or collagen vascular disorder that in the Investigator's opinion could interfere with the study or require medical attention that would interfere with the study.
  • History of cancer other than basal cell skin cancer
  • History of hypoglycemia
  • Current smokers, greater than 10 pack year history, or patients quitting less than 1 year prior to screening
  • History within the past year of excessive alcohol intake or drug addiction
  • History of respiratory infection requiring treatment with an antibiotic within 2 week prior to visit 1
  • Chronic intermittent use of inhaled, oral, intra-muscular, topical or intravenous corticosteroids within 4 weeks of visit 1
  • Inability to perform consistent spirometry or nitric oxide exhalation
  • Treatment with an experimental, non-approved drug, or investigational drug within the past 30 days
  • Known hypersensitivity to rosiglitazone
  • History of noncompliance to medical regimens and participants who are considered to be potentially unreliable

Treatment and study plan

rosiglitazone

Drug

2mg, 4mg, 8mg

Primary outcomes

  1. Methacholine Responsiveness as Assessed by PC20,

    Time frame: patients were assessed at baseline and at 12 weeks

    PC20 is the concentration of methacholine at which patients had a decrease in Forced Expiratory Volume in one second (FEV1) of 20%

Secondary outcomes

  1. Exhaled Nitric Oxide in Parts Per Billion (Ppb), Parts Per Billion

    Time frame: patients were assessed at baseline and 12 weeks

    Fraction Exhaled Nitric oxide was measured on each visit prior to bronchoprovocation by chemiluminescence using an analyzer.

  2. Forced Expiratory Volume in 1 Second (FEV1)

    Time frame: patients were assessed at baseline and 12 weeks

    FEV1 in liters

  3. Forced Expiratory Volume in One Second (FEV1) Percent Predicted

    Time frame: patients were assessed at baseline and 12 weeks

    Spirometry was performed on each visit according to American Thoracic Society guidelines. FEV1 percent predicted was measured.

Sponsors and collaborators

Lead sponsor

Creighton University

Other

Registry information

Official study title

The Effects of the PPARy Agonist Rosiglitazone on Airway Hyperreactivity

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Feb 13, 2008
Registry last updated
Sep 2, 2011

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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