Exhaled Breath Analysis in Human Subjects

NCT ID: NCT05456009

Last Updated: 2024-08-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

1500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-02-19

Study Completion Date

2026-03-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Identification of exhaled breath pattern of human subjects

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Breath analysis with mass spectormetry as a non-invasive method to identfy exhaled breath patterns.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Exhaled Breath Pattern After Medication Intake, in OSA Patients, or Other Pulmonary Diseases

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

No intervention

No intervention

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* \>= 18 years
* Informed consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Deep Breath Intelligence (DBI)

UNKNOWN

Sponsor Role collaborator

University of Zurich

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University Hospital Zurich

Zurich, Canton of Zurich, Switzerland

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Switzerland

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Malcolm Kohler, MD

Role: CONTACT

+41442551111

Noriane Sievi, MSc

Role: CONTACT

+41442559815

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Malcolm Kohler, MD

Role: primary

Noriane Sievi, MSc

Role: backup

+41442559815

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2019-00030

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Biomarkers in Dyspnea
NCT03056547 COMPLETED NA
Exploring Breathing Patterns
NCT04754490 SUSPENDED