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Recruiting NCT07361380

NCT07361380 Non-Invasive Testing Device for Anaemia

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Clinical Trial Summary
NCT ID NCT07361380
Status Recruiting
Phase
Sponsor University of Oxford
Condition Pregnancy
Study Type OBSERVATIONAL
Enrollment 300 participants
Start Date 2024-10-28
Primary Completion 2026-04-30

Eligibility & Interventions

Sex Female only
Min Age 16 Years
Max Age 50 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 300 participants in total. It began in 2024-10-28 with a primary completion date of 2026-04-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Anaemia (iron deficiency) arises from a reduction in the number of healthy red blood cells or the level of haemoglobin (Hb) (a protein inside red blood cells) necessary to effectively transport oxygen throughout the body. Anaemia is common among pregnant women. The gold standard for anaemia diagnosis still relies on laboratory blood tests, which come with limitations in terms of point-of-care capability, accessibility and quality. The investigators have developed a portable and user-friendly device capable of detecting anaemia rapidly and non-invasively and facilitating appropriate treatment by distinguishing anaemia due to iron deficiency from other causes. The device, named The Vascular Imaging Tool for the Auricle (VITA), utilises high-resolution imaging technology to capture detailed images of blood cells and small blood vessels within the human body. The objectives of this study are to assess VITA's performance of (haemoglobin (Hb)) testing and its ability to identify iron deficiency anaemia against the clinical gold standard of laboratory blood tests.

Eligibility Criteria

Inclusion Criteria: * Participant is willing and able to give informed consent for participation in the study. * Pregnant * Aged 16-50 years Exclusion Criteria: * Ear piercings that cannot be temporarily removed that would prevent the ability of the VITA device to take images of the ear blood vessels. * Ear piercings that would be visible on the ear blood vessel images

Contact & Investigator

Central Contact

Paul Leeson, PhD FRCP FESC

✉ paul.leeson@cardiov.ox.ac.uk

📞 +44(0)1865 226845

Frequently Asked Questions

Who can join the NCT07361380 clinical trial?

This trial is open to female participants only, aged 16 Years or older, up to 50 Years, studying Pregnancy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07361380 currently recruiting?

Yes, NCT07361380 is actively recruiting participants. Contact the research team at paul.leeson@cardiov.ox.ac.uk for enrollment information.

Where is the NCT07361380 trial being conducted?

This trial is being conducted at Oxford, United Kingdom.

Who is sponsoring the NCT07361380 clinical trial?

NCT07361380 is sponsored by University of Oxford. The trial plans to enroll 300 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology