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Zileuton to Treat Adults With Chronic Obstructive Pulmonary Disease (The LEUKO Study) (LEUKO)

Primary Purpose

Pulmonary Disease, Chronic Obstructive

Status
Terminated
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Zileuton
Placebo
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Disease, Chronic Obstructive focused on measuring Chronic Obstructive Pulmonary Disease, COPD, Exacerbation, Anti-leukotriene, Length of Stay, LOS

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Admitted to the hospital for a COPD exacerbation
  • FEV1 less than 60% of predicted level
  • At least 10 pack years of smoking

Exclusion Criteria:

  • Any uncontrolled systemic disease
  • Known hypersensitivity to zileuton
  • Asthma
  • Lobar pneumonia or pulmonary edema
  • Interstitial lung disease
  • Medical condition that is likely to limit survival to less than 30 days at the time of study entry
  • History of liver disease
  • Current use of theophylline
  • Participation in another clinical trial in the COPD Clinical Research Network
  • Incarceration
  • Institutionalization
  • Pregnant
  • History of a suicide attempt
  • Prior inpatient admission for a psychiatric disorder
  • Bipolar disorder

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Sites / Locations

  • University of Alabama Lung Health Center
  • Veteran's Administration Medical Center
  • LA BioMed at Harbor, University of California
  • University of California San Francisco-Airway Clinical Research Center
  • Denver Health Medical Center
  • National Jewish Medical and Research Center
  • Veteran's Administration Medical Center
  • University of Maryland Hospital
  • Fallon Clinic
  • Brigham and Women's Hospital
  • Veteran's Administration Medical Center
  • Veteran's Administration Medical Center
  • University of Michigan Medical Center
  • Veteran's Administration Medical Center
  • HealthPartners Research Foundation
  • Mayo Clinic
  • Temple University Lung Center
  • University of Pittsburgh Emphysema Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Zileuton

Placebo

Arm Description

Zileuton (Zyflo, 600 mg 4 times a day)

Placebo

Outcomes

Primary Outcome Measures

Length of Hospital Stay
Admission will begin at the time the subject has been admitted to an inpatient service. Length of Stay (LOS) will be recorded in days. The LOS will be based on the number of days spent in an acute medical ward or in the ICU. Subjects that are admitted and discharged in the same 24 hour period will be recorded as a LOS of 1 day, as will subjects discharged in the ensuing 24 hour period. LOS's greater than 10 days will be truncated to 10 days.

Secondary Outcome Measures

Change in FEV1% Predicted
Change in Post-bronchodilator FEV1% predicted comparing data at 30 day visit with baseline.
Change in FEV1/FEV6 Levels
Change in Post-bronchodilator FEV1/FEV6 ratio comparing data at discharge visit with baseline.
Treatment Failure
Treatment failure is defined as death, intubation, readmission to a hospital for COPD, urgent visit to an outpatient or ED provider for symptoms of COPD or intensification of therapy [including second course of antibiotics for COPD, and second course of systemic steroids for COPD]) in the first 30 days after randomization.
Health-related Quality of Life
St. George's Respiratory Questionnaire - Total Score The SGRQ was asked with respect to the last one month as validated for acute exacerbations of COPD by Doll et al. Scale from 0 (no disability) to 100 (maximum disability). The SGRQ total score summarizes the impact of airway specific disease on overall health status. Scores range from zero (no impairment) to 100 (maximum impairment). Scores were calculated using the SGRQ scoring Algorithm.
Change in Urinary Leukotriene (LTE4) Levels
Change in natural log-transformed LTE4 (ng/mg Cr.) from Baseline to 24 Hours
Change in Urinary Leukotriene (LTE4) Levels
Change in natural log-transformed LTE4 (ng/mg Cr.) from Baseline to 72 Hours

Full Information

First Posted
June 28, 2007
Last Updated
October 30, 2019
Sponsor
University of Minnesota
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT00493974
Brief Title
Zileuton to Treat Adults With Chronic Obstructive Pulmonary Disease (The LEUKO Study)
Acronym
LEUKO
Official Title
Antileukotriene Therapy for COPD Exacerbations
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Terminated
Why Stopped
Lack of feasibility due to low recruitment
Study Start Date
March 2007 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Chronic obstructive pulmonary disease (COPD) is a long-term lung disease that is caused by cigarette smoking or by breathing in other lung irritants, including pollution, dust, or chemicals. The purpose of this study is to evaluate the effectiveness of zileuton, a medication that is used to control asthma symptoms, at reducing the length of a hospital stay for adults who are hospitalized for a COPD exacerbation, or worsening of COPD symptoms.
Detailed Description
COPD is a disease in which the lung airways are partly damaged and obstructed, making it difficult to breathe. COPD is the fourth leading cause of death in the United States. Symptoms include coughing, excess mucus production, shortness of breath, wheezing, and chest tightness. Treatment usually includes inhaled bronchodilator or steroid medications that work by relaxing the muscles around the lung airways and reducing inflammation. Zileuton, a medication that is used to prevent asthma symptoms, may be beneficial in treating people who experience COPD exacerbations. Zileuton works by blocking the formation of substances that cause inflammation, fluid retention, and constriction in the lungs. The purpose of this study is to evaluate the effectiveness of zileuton at reducing the length of a hospital stay for adults who are hospitalized for a COPD exacerbation. This study will enroll adults who are admitted to the hospital due to severe COPD symptoms. Participants will be randomly assigned to receive either zileuton or placebo four times a day for up to 14 days. While in the hospital, lung function testing and urine collection will occur. Study visits will occur at Days 14 and 30, and will include lung function testing, a medical history review, and a study drug adverse effects review.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease, Chronic Obstructive
Keywords
Chronic Obstructive Pulmonary Disease, COPD, Exacerbation, Anti-leukotriene, Length of Stay, LOS

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
119 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Zileuton
Arm Type
Active Comparator
Arm Description
Zileuton (Zyflo, 600 mg 4 times a day)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
Zileuton
Other Intervention Name(s)
Zyflo
Intervention Description
Zyflo tablets, 600 mg, 4 times a day
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Inactive Matching Placebo
Intervention Description
Placebo 4 x daily
Primary Outcome Measure Information:
Title
Length of Hospital Stay
Description
Admission will begin at the time the subject has been admitted to an inpatient service. Length of Stay (LOS) will be recorded in days. The LOS will be based on the number of days spent in an acute medical ward or in the ICU. Subjects that are admitted and discharged in the same 24 hour period will be recorded as a LOS of 1 day, as will subjects discharged in the ensuing 24 hour period. LOS's greater than 10 days will be truncated to 10 days.
Time Frame
Measured at Day 30
Secondary Outcome Measure Information:
Title
Change in FEV1% Predicted
Description
Change in Post-bronchodilator FEV1% predicted comparing data at 30 day visit with baseline.
Time Frame
Measured at Baseline and Day 30
Title
Change in FEV1/FEV6 Levels
Description
Change in Post-bronchodilator FEV1/FEV6 ratio comparing data at discharge visit with baseline.
Time Frame
from baseline to day of discharge
Title
Treatment Failure
Description
Treatment failure is defined as death, intubation, readmission to a hospital for COPD, urgent visit to an outpatient or ED provider for symptoms of COPD or intensification of therapy [including second course of antibiotics for COPD, and second course of systemic steroids for COPD]) in the first 30 days after randomization.
Time Frame
Baseline to day 30 visit
Title
Health-related Quality of Life
Description
St. George's Respiratory Questionnaire - Total Score The SGRQ was asked with respect to the last one month as validated for acute exacerbations of COPD by Doll et al. Scale from 0 (no disability) to 100 (maximum disability). The SGRQ total score summarizes the impact of airway specific disease on overall health status. Scores range from zero (no impairment) to 100 (maximum impairment). Scores were calculated using the SGRQ scoring Algorithm.
Time Frame
Change from Baseline and 1 Month
Title
Change in Urinary Leukotriene (LTE4) Levels
Description
Change in natural log-transformed LTE4 (ng/mg Cr.) from Baseline to 24 Hours
Time Frame
Baseline and 24 hours
Title
Change in Urinary Leukotriene (LTE4) Levels
Description
Change in natural log-transformed LTE4 (ng/mg Cr.) from Baseline to 72 Hours
Time Frame
Baseline and 72 hours later

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Admitted to the hospital for a COPD exacerbation FEV1 less than 60% of predicted level At least 10 pack years of smoking Exclusion Criteria: Any uncontrolled systemic disease Known hypersensitivity to zileuton Asthma Lobar pneumonia or pulmonary edema Interstitial lung disease Medical condition that is likely to limit survival to less than 30 days at the time of study entry History of liver disease Current use of theophylline Participation in another clinical trial in the COPD Clinical Research Network Incarceration Institutionalization Pregnant History of a suicide attempt Prior inpatient admission for a psychiatric disorder Bipolar disorder '
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prescott Woodruff, MD
Organizational Affiliation
University of California at San Francisco
Official's Role
Study Chair
Facility Information:
Facility Name
University of Alabama Lung Health Center
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35249
Country
United States
Facility Name
Veteran's Administration Medical Center
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States
Facility Name
LA BioMed at Harbor, University of California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90502
Country
United States
Facility Name
University of California San Francisco-Airway Clinical Research Center
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
Denver Health Medical Center
City
Denver
State/Province
Colorado
ZIP/Postal Code
80204
Country
United States
Facility Name
National Jewish Medical and Research Center
City
Denver
State/Province
Colorado
ZIP/Postal Code
80206
Country
United States
Facility Name
Veteran's Administration Medical Center
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States
Facility Name
University of Maryland Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Facility Name
Fallon Clinic
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
01605
Country
United States
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Veteran's Administration Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02132
Country
United States
Facility Name
Veteran's Administration Medical Center
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48105
Country
United States
Facility Name
University of Michigan Medical Center
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Facility Name
Veteran's Administration Medical Center
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55417
Country
United States
Facility Name
HealthPartners Research Foundation
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55440
Country
United States
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
Temple University Lung Center
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19140
Country
United States
Facility Name
University of Pittsburgh Emphysema Research Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21299475
Citation
Woodruff PG, Albert RK, Bailey WC, Casaburi R, Connett JE, Cooper JA Jr, Criner GJ, Curtis JL, Dransfield MT, Han MK, Harnden SM, Kim V, Marchetti N, Martinez FJ, McEvoy CE, Niewoehner DE, Reilly JJ, Rice K, Scanlon PD, Scharf SM, Sciurba FC, Washko GR, Lazarus SC; Copd Clinical Research Network. Randomized trial of zileuton for treatment of COPD exacerbations requiring hospitalization. COPD. 2011 Feb;8(1):21-9. doi: 10.3109/15412555.2010.540273.
Results Reference
derived

Learn more about this trial

Zileuton to Treat Adults With Chronic Obstructive Pulmonary Disease (The LEUKO Study)

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