AzTrials
AzTrials

Respiratory Distress Syndrome, AdultNCT00217880

Significance of Biological Markers in Patients With Acute Lung Injury/Acute Respiratory Disease

A study testing Bronchoscopy in people with Respiratory Distress Syndrome, Adult, run by University of Michigan at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to identify biological markers of disease in patients with acute lung injury (ALI) that are predictive of either disease susceptibility or prognosis, or that identify novel targets of therapeutic intervention. Read more about this study

Who is it for?
Ages 18 to 95 years
Conditions the study is for
Respiratory Distress Syndrome, Adult
What is being tested?
Bronchoscopy
Type of treatment
Surgery or procedure
How many people
40 participants
Where
2 sitesUnited States
Study dates
Jul 2004to Jun 2009
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 95 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Acute onset of illness with:
  • PaO2/FiO2 ratio of less than 300 (ALI) or PaO2/FiO2 ratio of less than 200 (ARDS)
  • Bilateral infiltrates consistent with pulmonary edema on frontal chest radiograph (infiltrates may be patchy, diffuse, homogeneous, or asymmetric)
  • Positive pressure ventilation via an endotracheal tube
  • No clinical evidence of left atrial hypertension (if measured, pulmonary arterial wedge pressure less than or equal to 18 mm Hg)
  • First three criteria must occur together within a 24-hour interval

Who cannot join

  • Greater than 48 hours elapsed following institution of mechanical ventilation
  • Pregnancy
  • Chronic respiratory failure as defined by any of the following:
  • FEV1 less than 20 ml/kg of PBW; FEV1/FVC less than 50%
  • Chronic hypercapnia or hypoxemia
  • Hospitalization within past 6 months for acute respiratory failure
Show all 20Show fewer
  • Chronic home use of oxygen or mechanical ventilation
  • Left ventricular failure as defined by New York Heart Association (NYHA) class IV status
  • History of hematological malignancy or bone marrow transplantation
  • Entry in other intervention clinical trials
  • Decision of the patient or attending physician to forego aggressive care
  • Expected survival of less than 6 months (based solely on pre-existing medical problems [e.g., poorly controlled neoplasm or other end-stage disease])
  • AIDS (known history of HIV infection)
  • Prednisone (or equivalent) therapy of 20 mg/day or more for a period of at least 2 months with treatment continuing within 3 weeks prior to screening
  • Cytotoxic therapy within 3 weeks of screening
  • Morbid obesity defined as greater than 1 kg/c body weight
  • At risk for increased intracranial pressure that may result from permissive hypercapnia
  • Permissive hypercapnia that is contraindicated
  • Neuromuscular disease that would potentially impact ability to wean from mechanical ventilation
  • Receiving extracorporeal membrane oxygenation when meeting screening criteria

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • University of Michigan

    Ann Arbor, Michigan, 48109

  • Emory University

    Atlanta, Georgia, 30322

Other trials in United States

About this study

Official title: Prognostic Significance of Biological Markers in Patients With ALI/ARDS

The purpose of this study is to identify biological markers of disease in patients with acute lung injury (ALI) that are predictive of either disease susceptibility or prognosis, or that identify novel targets of therapeutic intervention.

Read the detailed description

BACKGROUND:

Respiratory failure due to ALI and acute respiratory distress syndrome (ARDS) remains a major health problem despite significant progress in intensive care unit (ICU) care and ventilator management. It is also characterized by an unacceptably high mortality rate despite enormous expenditure of health care resources. Survivors of respiratory failure face long-term consequences concerning their quality of life. New therapies are needed to improve early survival and to decrease long-term sequelae of this syndrome. The purpose of this study is to identify biological markers of disease in patients with ALI that are predictive of either disease susceptibility or prognosis, or that identify novel targets of therapeutic intervention.

DESIGN NARRATIVE:

As soon as possible after case identification, informed consent will be obtained from the patient or next of kin. Physiologic measurements and specimen collection will begin at the time of entry into the study. The inclusion criteria for this study allow entry of patients who have fulfilled criteria for ALI/ARDS for up to 48 hours. Bronchoalveolar lavage (BAL) fluid and blood will be collected at various times after the onset of ALI/ARDS in order to measure levels of a predetermined set of biological markers. In addition, DNA will be collected from patients and analysed for the presence of specific genetic polymorphisms that might alter either disease susceptibility or clinical expression of disease. The levels of these markers or the presence of specific genetic polymorphisms will be correlated with measure of pulmonary inflammation and extent of lung injury, as defined by: 1) PaO2/FiO2 ratios; 2) lung compliance; 3) plateau pressures; and 4) calculation of the Murray Lung Injury Score (obtained at entry and Days 1, 2, 3, 5, 7,10, 14, and 21). Secondary outcome measures to be directly correlated with biomarker expression will include indicators of maladaptive responses to ALI (including the development of multiple organ dysfunction syndrome [MODS]), fibroproliferation, and nosocomial pneumonia (events which greatly impact the clinical course of patients with ALI/ARDS). Thus, the secondary outcome measures include: 1) the development of organ failure (using the Sequential Organ Failure Assessment [SOFA] score); 2) time on ventilator; 3) ventilator-free days; 4) ICU and hospital length of stay; 5) hospital mortality; 6) development of pneumonia; 7) development of lung fibrosis (as determined by high-resolution computed tomography [HRCT] and pulmonary function testing); and 8) health related and lung-specific quality of life (as assessed with the Medical Outcome Studies 36-Item Short form Health Survey Standard Form [SF-36] and St. George's Respiratory Questionnaire).

Being tested
Bronchoscopy
Medical subject headings
Respiratory Distress Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BronchoscopyProcedure or surgery

    A bronchoscopy test will occur to view the participant's airways.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. PaO2/FiO2 ratios

    Measured: Measured at Year 4

  2. Lung compliance

    Measured: Measured at Year 4

  3. Plateau pressures

    Measured: Measured at Year 4

  4. Calculation of the Murray Lung Injury Score (obtained at entry and Days 1, 2, 3, 5, 7,10, 14, and 21; analyzed at Year 4)

    Measured: Measured at Year 4

Secondary outcomes (8)
  1. Development of organ failure

    Measured: Measured at Year 4

  2. Time on ventilator

    Measured: Measured at Year 4

  3. Ventilator-free days

    Measured: Measured at Year 4

  4. ICU and hospital length of stay

    Measured: Measured at Year 4

  5. Hospital mortality

    Measured: Measured at Year 4

  6. Development of pneumonia

    Measured: Measured at Year 4

  7. Development of lung fibrosis

    Measured: Measured at Year 4

  8. Health-related and lung-specific quality of life

    Measured: Measured at Year 4

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Sep 2005 (estimated)
  2. Study startJul 2004
  3. Primary completionApr 2009
  4. Study completionJun 2009

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00217880
Sponsor's protocol ID
292
Other IDs
P50HL074024
Status last verified
Jul 2009
First submitted
19 Sep 2005
Last updated
19 Aug 2013
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A study testing Bronchoscopy in people with Respiratory Distress Syndrome, Adult, run by University of Michigan at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 20 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Aug 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

PaO2/FiO2 ratios (time frame: Measured at Year 4). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Aug 2013.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in