Completed

Phase 3
Age: 13Years +
All Genders
ID00000579

Acute Respiratory Distress Syndrome Clinical Network (ARDSNet)

Led by National Heart, Lung, and Blood Institute (NHLBI) ยท Updated on 2016-03-23

N/A

Participants Needed

21

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Official Title

Acute Respiratory Distress Syndrome Clinical Network (ARDSNet)

Who Can Participate

Age: 13Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

Inclusion Criteria:

  • Men and women
  • 13 years of age or older
  • ARDS or risk factors for ARDS (patients will be considered at risk if they are critically ill and have trauma, sepsis, shock, pneumonia, inhalation injury, drug overdose, pancreatitis, or hypertransfusion)
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

Trial Site Locations

Total: 21 locations

1

University of California

San Francisco, California, United States, 94143

Status Unknown

2

University of Colorado Health Sciences Center

Denver, Colorado, United States, 80262

Status Unknown

3

University of Chicago

Chicago, Illinois, United States, 60637

Status Unknown

4

Louisiana State University

New Orleans, Louisiana, United States, 70112

Status Unknown

5

University of Maryland

Baltimore, Maryland, United States, 21201

Status Unknown

6

Massachusetts General Hospital

Boston, Massachusetts, United States, 02114

Status Unknown

7

Baystate Medical Center

Springfield, Massachusetts, United States, 01199

Status Unknown

8

University of Michigan

Ann Arbor, Michigan, United States, 48109

Status Unknown

9

Mayo Foundation

Rochester, Minnesota, United States, 55905

Status Unknown

10

Duke University

Durham, North Carolina, United States, 27708

Status Unknown

11

Wake Forest University

Winston-Salem, North Carolina, United States, 27157

Status Unknown

12

Cleveland Clinic Foundation

Cleveland, Ohio, United States, 44195

Status Unknown

13

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Status Unknown

14

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15261

Status Unknown

15

Vanderbilt University

Nashville, Tennessee, United States, 37232

Status Unknown

16

Baylor College of Medicine

Houston, Texas, United States, 77030

Status Unknown

17

University of Texas

San Antonio, Texas, United States, 78229-3900

Status Unknown

18

Latter Day Saints Hospital

Salt Lake City, Utah, United States, 84143

Status Unknown

19

University of Virginia

Charlottesville, Virginia, United States, 22908

Status Unknown

20

University of Washington

Seattle, Washington, United States, 98105

Status Unknown

21

University of British Columbia

Vancouver, British Columbia, Canada, V5Z 1M9

Status Unknown

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

N/A

Allocation

N/A

Model

FACTORIAL

Primary Purpose

TREATMENT

Number of Arms

0

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Published Research Related To This Trial

Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome.

Acute Respiratory Distress Syndrome Network, Roy G Brower, Michael A Matthay...

https://pubmed.ncbi.nlm.nih.gov/10793162

Efficacy of low tidal volume ventilation in patients with different clinical risk factors for acute lung injury and the acute respiratory distress syndrome.

M D Eisner, T Thompson, L D Hudson...

https://pubmed.ncbi.nlm.nih.gov/11463593

Recovery rate and prognosis in older persons who develop acute lung injury and the acute respiratory distress syndrome.

E Wesley Ely, Arthur P Wheeler, B Taylor Thompson...

https://pubmed.ncbi.nlm.nih.gov/11777361

Implementation of a low tidal volume ventilation protocol for patients with acute lung injury or acute respiratory distress syndrome.

R H Kallet, W Corral, H J Silverman...

https://pubmed.ncbi.nlm.nih.gov/11572755

Statistical evaluation of ventilator-free days as an efficacy measure in clinical trials of treatments for acute respiratory distress syndrome.

David A Schoenfeld, Gordon R Bernard, ARDS Network

https://pubmed.ncbi.nlm.nih.gov/12163791
Acute Respiratory Distress Syndrome Clinical Network (ARDSNet) | DecenTrialz