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Terminated Phase 3 Interventional Results available

Beta-Blockers for the Prevention of Acute Exacerbations of Chronic Obstructive Pulmonary Disease

ClinicalTrials.gov ID: NCT02587351

Public ClinicalTrials.gov record NCT02587351. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 11:44 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Beta-Blockers for the Prevention of Acute Exacerbations of COPD

Study identification

NCT ID
NCT02587351
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
University of Minnesota
Other
Enrollment
532 participants

Conditions and interventions

Interventions

  • Metoprolol succinate Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
40 Years to 84 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2016
Primary completion
Aug 31, 2019
Completion
Nov 30, 2019
Last update posted
Jan 24, 2021

2016 – 2019

United States locations

U.S. sites
27
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Birmingham, Alabama VA Medical Birmingham Alabama 35233
University of Alabama at Birmingham Birmingham Alabama 35294
University of California, San Francisco-Fresno Fresno California 93701
LA BioMed at Harbor-UCLA Medical Center Los Angeles California 90502
University of California at San Francisco San Francisco California 94143
National Jewish Medical & Research Center Denver Colorado 80206
North Florida/South Georgia Veterans Health System Gainesville Florida 32608
Northwestern University Chicago Illinois 60611
Louisiana State University New Orleans Louisiana 70112
University of Maryland Baltimore Baltimore Maryland 21201
Brigham and Women's Hospital Boston Massachusetts 02115
VA Ann Arbor Healthcare System Ann Arbor Michigan 48105
University of Michigan Ann Arbor Michigan 48109
Veteran's Administration Medical Center Minneapolis Minnesota 55417
HealthPartners Research Foundation Minneapolis Minnesota 55440
Mayo Clinic Rochester Minnesota 55905
NewYork-Presbyterian Brooklyn Methodist Hospital Brooklyn New York 11215
New York Presbyterian/Queens Flushing New York 11355
Cornell University Ithaca New York 14853
Columbia University New York New York 10027
Cincinnati VA Medical Center Cincinnati Ohio 45220
Cleveland Clinic Cleveland Ohio 44195
Temple University Lung Center Philadelphia Pennsylvania 19140
University of Pittsburgh Pittsburgh Pennsylvania 15213
University of Utah Health Sciences Center Salt Lake City Utah 84132-4701
The University of Vermont Burlington Vermont 05405
University of Washington School of Medicine Spokane Washington 99258

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02587351, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 24, 2021 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02587351 live on ClinicalTrials.gov.

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