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Status unknownNCT01503723Updated Jan 4, 2012

Biomarkers in Exhaled Breath Condensates in Acute Lung Injury: Early Detection and Outcome Predictors

An observational study in Acute Lung Injury, sponsored by National Taiwan University Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-01-04.

Sponsored by National Taiwan University Hospital · Observational

The sponsor has not verified this record recently (last verified Sep 2011), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
300
Ages
18 Years and older
Sex
All
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Study summary

Metabolomics, or metabonomics, is a large-scale approach to monitoring as many as possible of the compounds involved in cellular processes in a single assay to derive metabolic profiles. Metabolomics allows for a global assessment of a cellular state within the context of the immediate environment, taking into account genetic regulation, altered kinetic activity of enzymes, and changes in metabolic reactions. Metabolomics may be useful for understanding metabolic imbalances and for diagnosis of human disease. The investigators plan to collect exhaled breath condensate from patients with acute lung injury. Metabolomic analysis in the patients may help us to explore some novel biomarkers for the disease diagnosis and outcome prediction.

Read the detailed description

Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are the leading causes of mortality and morbidity in the intensive care unit (ICU). The causes of ALI/ARDS differ from patient to patient, including sepsis, aspiration, systemic inflammation, trauma, blood transfusion, etc. With early detection and treatment, the survival rate may be improved significantly. However, it is often difficult to differentiate ALI/ARDS from cardiogenic pulmonary edema or other causes, even with advanced technology and invasive tools. A potential tool is the breath chemical test, ranging from exhaled gas measurement, such as exhaled nitric oxide or carbonic monoxide, to volatile organic compound determination and nonvolatile biomarker profiling. Being completely noninvasive, sampling of the exhaled breath condensates (EBC) allows clinicians and researchers to assess body functions in an easier and flexible manner. Exhaled breath contains thousands of volatile and nonvolatile compounds in trace amounts. Therefore, it is not until recently, after the development of highly sensitive cutting-edge technologies in sample analysis, that the evaluation of this type of human specimens becomes possible. Advanced technologies in proteomics, metabolomics, GC/LC-Mass Spectrometry and pattern recognition computation generate a field of exhaled biomarker profiling, called "breathomics." After the establishment of the metabolomic profiling of EBC in patients with ALI, ARDS or cardiogenic pulmonary edema, a useful and powerful noninvasive tool for ALI/ARDS diagnosis and outcome prediction could be set up.

Metabolomics, or metabonomics, is a large-scale approach to monitoring as many as possible of the compounds involved in cellular processes in a single assay to derive metabolic profiles. Although metabolomics first referred to the monitoring of individual cells and metabonomics referred to multicellular organisms, these terms are now often used interchangeably. Metabolic changes occur through a number of mechanisms, including direct genetic regulation and alterations in enzymatic and metabolic reactions. Metabolomics allows for a global assessment of a cellular state within the context of the immediate environment, taking into account genetic regulation, altered kinetic activity of enzymes, and changes in metabolic reactions. Thus, compared with genomics or proteomics, metabolomics reflects changes in phenotype and therefore function. Techniques applied to metabolic profiling include nuclear magnetic resonance (NMR) and mass spectrometry (MS). Metabolomics have the advantage of being capable of searching for proteins or metabolites in the blood or urine. Metabolomics may be useful for understanding metabolic imbalances and for diagnosis of human disease. Over 30 endogenous metabolites have been studied in breast tissue, and breast cancer show elevated total choline-containing compounds (tCho), low glycerophosphocholine, and low glucose compared with benign tumors or healthy tissue. Similar to breast cancer, prostate cancer exhibits a distinct metabolic profile characterized by high tCho and phosphocholine levels, along with an increase in the glycolytic products lactate and alanine. In prostate cancer, citrate may also be a marker of responsiveness to treatment. These results show the potential utility of metabolomics in cancer diagnosis and clinical evaluation.

Breath chemical tests have a broad spectrum of applications ranging from exhaled nitric oxide fraction (FeNO) measurement to monitor the effect of anti-inflammatory treatment in asthma, to volatile organic compound (VOC) determination and nonvolatile biomarker profiling in the cooled breath sample called exhaled breath condensate (EBC). Being completely noninvasive, sampling of the breath allows clinicians and researchers to assess different body functions in a flexible manner. Therefore, breath testing is considered to be a potentially ideal candidate for screening purposes. Besides widely known constituents such as nitrogen, oxygen, carbon dioxide, inert gases and water vapour, exhaled breath also consists of thousands of volatile and nonvolatile components, mainly in trace amounts, making detection a challenging task. The use of innovative "-omics" technologies, including proteomics, metabolomics, mass spectromics, gas chromatography/mass spectrometry (GC-MS) and ion mobility spectrometries, offers great potential for the field of exhaled biomarker profiling. Unlike bronchoalveolar lavage (BAL) and sputum induction which involves inhalation of hypertonic saline to induce cough and possibly bronchoconstriction, EBC does not influence airway function or cause inflammation. It can be easily and safely performed on patients with severe illness and even allows for repeated measurements to be taken. As such, this is a relatively new field with potential for more studies to be performed to investigate acute lung injury by metabolomics.

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Conditions studied

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In context

Lung Injury

399 studies on the registry are indexed under Lung Injury; 50 are open to participants now.

This study's planned enrollment of 300 is above the median of 70 across 136 observational studies indexed under Lung Injury.

Browse Lung Injury studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients who are admitted to ICU with the diagnosis of acute hypoxemic respiratory failure and endotracheally intubated with mechanical ventilation.

Inclusion criteria

  • above 18 years old
  • admitted to ICU with the diagnosis of acute hypoxemic respiratory failure and endotracheally intubated with mechanical ventilation.

Exclusion criteria

Exclusion Criteria:

  • pregnancy
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
300 participants (estimated)
Biospecimen retention
Samples without dna

Groups and cohorts

  • Patients with acute lung injury

    Patients who are admitted to ICU with the diagnosis of acute hypoxemic respiratory failure

    Other: Determined by intended physician

Interventions

  • OtherDetermined by intended physician

    We perform a prospective observational study. All the treatment for the patients are determined by intended physicians.

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What researchers measure

Primary outcomes

  1. Diagnosis

    To differentiate ALI/ARDS from cardiogenic pulmonary edema or other causes

    Time frame: 28 days

  2. Disease severity

    Time frame: 28 days

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Study locations

1 of 1 sites recruiting
  • National Taiwan University Hospital
    Taipei, Taiwan
    • Lu-Cheng Kuo, MD, Master · Contact · kuolc@ntu.edu.tw · 886-2-23562905
    • Lu-Cheng Kuo, MD, Master · Principal investigator
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 4, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01503723
Lead sponsor
National Taiwan University Hospital
Responsible party
Sponsor
First posted
Jan 4, 2012
Start date
Aug 2011
Last update
Jan 4, 2012

Study contacts

Lu-Cheng Kuo, MD, Master
Contact
kuolc@ntu.edu.tw
886-2-23562905
Lu-Cheng Kuo, MD, Master
principal investigator · National Taiwan University Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2011. You cannot join it, but the record below documents what was studied.

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