LHSII: Lung Health Study II

Sponsor
University of Minnesota (Other)
Overall Status
Completed
CT.gov ID
NCT00000569
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
1,116
2
67.9

Study Details

Study Description

Brief Summary

To determine if participants with chronic obstructive pulmonary disease, who were assigned to inhaled corticosteroids had a lower rate of decline in lung function and lower incidence of respiratory morbidity compared to participants assigned to placebo.

Condition or Disease Intervention/Treatment Phase
Phase 3

Detailed Description

BACKGROUND:

Chronic obstructive pulmonary disease (COPD), the fourth leading cause of death in the United States and a major cause of morbidity, is a spectrum of chronic lung diseases including clinical diagnoses of chronic bronchitis, emphysema, and combinations of both. Varying degrees of bronchoreactivity occur over the entire spectrum. Asthma and COPD have many features in common. Distinction is usually dependent on clinical features and clinical course. The diagnosis of asthma will not exclude a patient from the designation of COPD for this study, although criteria for exclusion include recent (within six months) use of inhaled or oral steroid with the intent of excluding most of those who are clearly predominantly bronchospastic. The morbid anatomy of COPD is well described and includes many features of acute and chronic inflammation. There is well supported evidence in the literature that this inflammatory process may be an important pathogenetic mechanism in the development of emphysema. On this basis, the rationale for the use of corticosteroids is well justified. There are various published studies suggesting that inhaled steroids reduce bronchial lavage markers of inflammation, variously influence short-term bronchial hyperreactivity, improve lung function acutely or short-term, and slow rate of decline in lung function. Most studies have asked for improvement rather than stability. However, despite the studies which do not support these contentions and the lack of long-term information, inhaled steroids in COPD are becoming widely used in clinical practice. It was the intent of this clinical trial to assess the long-term efficacy of this treatment before such therapy became an accepted community practice, making it impractical or impossible to conduct a clinical trial.

DESIGN NARRATIVE:

Subjects were recruited from the Lung Health Study I and randomized to 1200 micrograms of triamcinolone in daily divided doses or to placebo. Pulmonary function was evaluated every six months. Bronchial activity was tested at baseline, at nine months, and at three-and-a-half years using a methacholine inhalation challenge. Mean duration of follow-up was 40 months. The primary outcome measure was the rate of decline in pulmonary function as assessed by the post-bronchodilator forced expiratory volume at one second (FEV1) value. Other outcome measures included death, respiratory symptoms, quality of life, side-effects and toxicity, adherence, bronchial hyperreactivity, atopic status, and smoking status. Recruitment was initiated in November 1994 and ended November 28, 1995 to allow 3.5 to 4.5 years of follow-up through April, 1999.

The investigators initiated a dose monitor (puff counter) protocol at nine of the centers among the fair to satisfactory compliers (4 to 9 puffs versus the ideal of 12 puffs per day) to test whether a memory aid would enhance inhaler compliance. Consenting participants were randomized to Group 1 who could see the display on the puff counter for 12 months or to Group 2 who had no counter for three months, a counter that recorded but did not display for three months, and a counter with display for six months.

There were a bone densitometry and adrenal suppression ancillary studies, funded by Rhone-Poulenc-Rorer, to assess the effect of inhaled corticosteroids on bone density and adrenal function.

Study Design

Study Type:
Interventional
Actual Enrollment :
1116 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Chronic Obstructive Pulmonary Disease Early Intervention Trial
Study Start Date :
Sep 1, 1993
Actual Primary Completion Date :
May 1, 1999
Actual Study Completion Date :
May 1, 1999

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Triamcinolone

1200 micrograms of triamcinolone in daily divided doses

Drug: triamcinolone
1200 micrograms of triamcinolone in daily divided doses
Other Names:
  • Azmacort
  • Placebo Comparator: Placebo

    Placebo

    Other: Placebo
    Placebo

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      40 Years to 69 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion:
      1. Previously participated in or screened for the Lung Health Study I

      2. Ages 40 to 69

      3. Forced expiratory volume at one second (FEV1)/forced vital capacity(FVC) < 70 percent

      4. Forced expiratory volume at one second (FEV1) 30 to 90 percent predicted.

      Exclusions:
      1. Cancer

      2. Recent myocardial infarction

      3. Alcoholism

      4. Heart Failure

      5. Insulin-dependent diabetes mellitus

      6. Neuropsychiatric disorders

      7. Used bronchodilators or oral or inhaled corticosteroids in previous year

      Contacts and Locations

      Locations

      No locations specified.

      Sponsors and Collaborators

      • University of Minnesota
      • National Heart, Lung, and Blood Institute (NHLBI)

      Investigators

      • Principal Investigator: John Connett, University of Minnesota

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      University of Minnesota
      ClinicalTrials.gov Identifier:
      NCT00000569
      Other Study ID Numbers:
      • 9109M04382
      • 5U01HL050267-03
      First Posted:
      Oct 28, 1999
      Last Update Posted:
      Nov 1, 2019
      Last Verified:
      Oct 1, 2019
      Individual Participant Data (IPD) Sharing Statement:
      No
      Plan to Share IPD:
      No
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Nov 1, 2019