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NCT Number: NCT07361380

Non-Invasive Testing Device for Anaemia

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.

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Key information

Age range

16 year–50 year

Sex eligibility

Female

Study type

Observational

Primary location

About this study

Anaemia arises from a reduction in the number of healthy red blood cells or the level of haemoglobin necessary to transport oxygen effectively throughout the body. It is a significant global health concern, affecting 1.6 billion individuals worldwide and untreated anaemia can contribute to chronic heart failure and chronic kidney disease. Anaemia is common among pregnant women. Mild cases of anaemia often go unnoticed due to their nonspecific symptoms, such as fatigue, headaches, and hair loss. Furthermore, studying this disease can be difficult as, particularly in places without ready access to laboratory blood sample analysis as current point-of-care solutions are not able to distinguish between different types of anaemia and prescribe suitable treatments. 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 biases related to poor standardisation of assays and low sample 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 vessels within the human body. Unlike existing non-invasive devices that can only measure properties in bulk tissue samples, VITA can analyse characteristics of hundreds of individual cells, thereby facilitating rapid point-of-care testing for iron deficiency anaemia. VITA is a low-cost device, and its unique ability to measure these parameters without requiring consumables or trained operators makes it particularly well-suited for researching anaemia in a range of settings, including low- and middle-income countries.

This project is a proof-of-concept study to assess VITA's performance of Hb testing. Secondary objectives include testing VITA's ability to identify iron deficiency anaemia against the clinical gold standard of laboratory blood tests, identification of other frequently measured blood biomarkers, and identification of biomarkers for long-term health. This study is not collecting data for licensing of the device.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. To compare Hb measured by VITA with Hb measured by blood sample analysis

    Time frame: Baseline

    Agreement between the two measurements as calculated by systemic error (bias), and 95% limits of agreement as bias ±2 SD concentration of haemoglobin in the blood in g/dl of VITA and blood sample analysis

Secondary outcomes

  1. To determine the maximum accuracy of VITA in detecting iron deficiency anaemia as compared to diagnosis based on guidelines on full iron studies in blood sample analysis

    Time frame: Baseline

    Accuracy of VITA algorithmic diagnosis (yes/no) compared to diagnosis (yes/no) based on haemoglobin, soluble transferrin receptor (sTfR), RDW (red cell distribution width), ferritin, serum iron, transferrin saturation (TSAT), mean corpuscular volume (MCV) and/or mean corpuscular haemoglobin concentration (MCHC)

  2. To train image processing software to detect biomarkers that are frequently used in clinical practice based on VITA images

    Time frame: Baseline

    Correlation of VITA algorithmic metrics and blood sample analysis metrics of the following biomarkers:

    • Folate
    • Renal function
    • Electrolytes
    • Liver function
    • Calcium phosphate
    • Thyroid function
    • Full blood count
    • Glucose
    • Insulin
    • Lipids
    • HbA1C
  3. To predict long-term health outcomes from features in VITA images

    Time frame: 6 months post-partum

    Medical records will be checked up to 6 months post-partum to check for the following indications:

    • Hypertensive disorders of pregnancy (gestational hypertension, pre-eclampsia, HELLP)
    • Other pregnancy complications
    • Blood pressure
    • Post-partum medical complications

Study contacts

Contact information is provided by the study sponsor or research team.

Paul Leeson, PhD FRCP FESC

CONTACT

[email protected]

+44(0)1865 226845

Sponsors and collaborators

Lead sponsor

University of Oxford

Other

Registry information

Official study title

Non-Invasive Testing of Blood Biomarkers in Pregnant Women

Acronym: NITA

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Jan 23, 2026
Registry last updated
Jan 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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