Acute Respiratory Distress Syndrome Clinical Network (ARDSNet)
NCT00000579 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL
Last updated 2016-03-23
Summary
The purposes of this study are to assess rapidly innovative treatment methods in patients with adult respiratory distress syndrome (ARDS) as well as those at risk of developing ARDS and to create a network of interactive Critical Care Treatment Groups (CCTGs) to establish and maintain the required infrastructure to perform multiple therapeutic trials that may involve investigational drugs, approved agents not currently used for treatment of ARDS, or treatments currently used but whose efficacy has not been well documented.
Conditions
- Respiratory Distress Syndrome, Adult
- Lung Diseases
Interventions
- PROCEDURE
-
Low Tidal Volume Ventilation
- PROCEDURE
-
Positive End-Expiratory Pressure
- DRUG
-
Lysofylline
- DRUG
-
Methylprednisolone
- DRUG
-
Ketoconazole
- PROCEDURE
-
Fluid Management
- PROCEDURE
-
Pulmonary Artery Catheter
Sponsors & Collaborators
-
National Heart, Lung, and Blood Institute (NHLBI)
lead NIH
Principal Investigators
-
Edward Abraham, MD · University of Colorado, Denver
-
Antonio Anzueto, MD · University of Texas
-
Roy Brower, MD · Johns Hopkins University
-
Alfred F. Connors, MD · University of Virginia
-
Bennett P. deBoisblanc, MD · Louisiana State University Health Sciences Center in New Orleans
-
Bennett P. deBoisblanc, MD · Louisiana State University Health Science Center
-
Michael Donahoe, MD · University of Pittsburgh
-
Kalpalatha K. Guntupalli, MD · Baylor College of Medicine
-
Robert D. Hite, MD · Wake Forest University
-
Robert D. Hite, MD · Wake Forest University Health Sciences
-
Rolf Hubmayr, MD · Mayo Clinic
-
Neil MacIntyre, MD · Duke University
-
Michael A. Matthay, MD · University of California, San Francisco
-
Alan Morris, MD · Latter Day Saints Hospital
-
Michael J. Murray · Mayo Foundation
-
James A. Russell, MD · University of British Columbia
-
Gregory A. Schmidt, MD, FCCP · University of Chicago
-
David A. Schoenfeld, PhD · Massachusetts General Hospital
-
Jay S. Steingrub, MD, FCCP · Baystate Medical Center
-
Arthur Wheeler, MD · Vanderbilt University
-
Herbert Wiedemann, MD · Cleveland Clinic Lerner College of Medicine
Study Design
- Purpose
- TREATMENT
- Model
- FACTORIAL
Eligibility
- Min Age
- 13 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1994-09-30
- Completion
- 2004-07-31
Countries
- United States
- Canada
Study Locations
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