An observational study in Technical Feasibility and Performance of the Sensor System, Healthy Adult and Healthy Adult Participants, sponsored by Bosch Quantum Sensing GmbH. Recruiting at 1 site in Germany. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-06.
Sponsored by Bosch Quantum Sensing GmbH · Observational
This prospective, single-center, exploratory feasibility study investigates the use of diamond-based nitrogen-vacancy (NV) magnetometers for non-invasive magnetocardiography (MCG). The goal is to assess whether highly sensitive NV sensors can reliably detect and reconstruct the weak magnetic fields generated by the human heart and evaluate their potential for future cardiac diagnostics.
This is the only study on the registry with Bosch Quantum Sensing GmbH as lead sponsor.
Counted across the registry records on this site, refreshed daily.
The study population consists of healthy adult volunteers recruited from employees of Robert Bosch GmbH (Corporate Research and Advanced Engineering) and Bosch Quantum Sensing GmbH.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Participants will undergo non-invasive cardiac magnetic field measurements using an array of diamond nitrogen-vacancy (NV) magnetometers.
Reconstruction of Cardiac Magnetic Field Maps
* Are the magnetic field signals (on the basis of the single sensor) recorded with the NV Application Kit in accordance with literature in terms of amplitude (in pT) and duration (in ms) of the p-wave, QRS-complex, T-wave? * Are the magnetic field maps recorded with the NV Application Kit in accordance with literature in terms of the number, location, and amplitude of magnetic poles?
Time frame: up to two weeks
Plan to share: Undecided
No publications or documents are linked to this record.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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