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Application of Nanotechnology and Chemical Sensors for Diagnosis of Decompensated Heart Failure by Respiratory Samples

Application of Nanotechnology and Chemical Sensors for Diagnosis of Decompensated Heart Failure by Respiratory Samples

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03083717
Enrollment
150
Registered
2017-03-20
Start date
2017-04-20
Completion date
2020-01-01
Last updated
2017-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Brief summary

Application of Nanotechnology and Chemical Sensors for Diagnosis of Decompensated Heart Failure by Respiratory Samples. Breath testing, which links specific volatile molecular biomarkers in exhaled breath to medical conditions, is becoming increasingly popular as a non-invasive and potentially inexpensive diagnostic method for various diseases. NA-NOSE performs odor detection from exhaled breath, thus producing a distinct fingerprint for each mixture of analytes. Several studies have been published, stating the advantages of these sensors, leading to promising outcomes in several fields. The NA-NOSE breath test would be fast (examination and results would be obtained within 5-10 min), inexpensive, eventually portable (smaller than desktop computer), non-invasive and free of any side effects.

Interventions

DIAGNOSTIC_TESTCollection of breath samples, followed by analysis of exhaled breath using nanomaterial-based sensors (NaNose)

2-3 liters of breath sample will be collected in chemically inert Mylar bags. The breath samples will then be immediately transferred from the Mylar bags to Tenax sorbent tubes using a dedicated pump. Tubes will be sealed and kept in 4˚C until NA-NOSE analysis.

Sponsors

Rambam Health Care Campus
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* signed informed consent * ≥ 18 years of age, male or female * Left ventricular Ejection fraction less than 40% or known to suffer from heart failure with preserved ejection fraction * In decompensated heart failure group: dyspnea with confirmation of pulmonary congestion/edema by chest x-ray

Exclusion criteria

* Pericardial diseases, e.g. constrictive pericarditis, tamponade * Significant congenital heart disease, up to the investigator's opinion * Life-threatening or uncontrolled arrhythmia, including symptomatic or sustained ventricular tachycardia and atrial fibrillation or flutter with a resting ventricular rate \>110 beats per minute. * Acute ST elevation myocardial infarction * Pregnant women * Patients with pulmonary embolism * Probable alternative diagnoses that in the opinion of the investigator could account for patient's HF symptoms (i.e., dyspnea), such as: 1. significant pulmonary disease 2. anemia with hemoglobin \<10 g/dl * participation in another study

Design outcomes

Primary

MeasureTime frameDescription
Detection of volatile organic compounds in breath samplesEach participant's breath sample will be analysed within one week of collection.Exhaled breath samples will be collected from each volunteer for characterization and identification using two different methods. The first method uses gas chromatography linked to mass spectrometry to identify and quantify the various breath volatile organic compunds (VOC's) in each group studied (compensated heart failure, decompensated heart failure and healthy subjects). The second method deploys cross-reactive nanoarrays in combination with pattern recognition methods (NaNose Technology).

Countries

Israel

Contacts

Primary ContactManhal A Habib, MD, PhD
Manhal.habib@gmail.com97247772180

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026