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Terminated Phase 3 Interventional

Calfactant for Direct Acute Respiratory Distress Syndrome

ClinicalTrials.gov ID: NCT00682500

Public ClinicalTrials.gov record NCT00682500. 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 Oct 22, 2026, 8:23 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

Calfactant Therapy for Direct Acute Respiratory Distress Syndrome & Direct Acute Lung Injury in Adults and Children

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will determine if administration of an suspension of calfactant, a lung surfactant, intratracheally in patients with Direct Acute Respiratory Distress Syndrome within 48 hours of requiring mechanical ventilation can decrease the mortality in patients with lethal disease and shorten the course of respiratory failure in patients with sub-lethal disease.

Study identification

NCT ID
NCT00682500
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
332 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years to 85 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
May 2008 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Feb 2011 (Actual)
Last update posted
Jul 24, 2012

2008 – 2011

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
University of Florida Gainesville Florida — —
Florida Hospital and Florida Children's Hospital Orlando Florida — —
Northwestern University-Chicago Chicago Illinois — —
West Suburban Hospital Medical Center Oak Park Illinois — —
Peoria Pulmonary Associates/OSF St. Francis Hospital Peoria Illinois — —
Clarian Health, Inc/Methodist Hospital Indianapolis Indiana — —
University of Iowa Iowa City Iowa — —
Creighton University Omaha Nebraska 68131 —
Omaha Children's Hospital Omaha Nebraska 68198 —
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire — —
Columbia Medical Center--Pediatrics New York New York — —
The Oregon Clinic Portland Oregon — —
Penn State University Hershey Pennsylvania — —
Baylor College of Medicine/Texas Children's Hospital Houston Texas — —
Uthscsa/Stvah San Antonio Texas — —
University of Virginia Health Science Center Charlottesville Virginia 22908 —
INOVA Fairfax Hospital Fairfax Virginia — —
Medical College of Wisconsin Milwaukee Wisconsin — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00682500, 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 Jul 24, 2012 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00682500 live on ClinicalTrials.gov.

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