Clinical Trials in Poland / NCT06973317
Starting soon Observational

Self-Powered Photodetectors for Smarter Healthcare

NCT06973317 · tracked via the Priya Life Science Poland tracker
Sponsor
Wrocław University of Science and Technology
Phase
Observational
Started
2027-06
Last updated
2025-07-10

Condition(s) studied

Blood Glucose Monitoring

Study summary

The goal of this observational study is to evaluate the performance of a novel, non-invasive sensor device based on zirconium oxide photodetector designed to monitor key physiological parameters: blood glucose levels, heart rate, and blood oxygen saturation. The study focuses on adult hospital patients aged 18 to 75, of all sexes, who are undergoing routine monitoring and treatment unrelated to the investigational device.

The main questions this study aims to answer are:

To what extent do the signals obtained from the newly developed device correlate with standard hospital-based methods for measuring blood glucose, heart rate, and blood oxygen saturation?

Is the device feasible, safe, and accurate for use in a real-world clinical setting?

How stable and reproducible are the sensor signals across a demographically diverse patient population?

Can advanced data analysis methods, such as machine learning techniques, be used effectively to interpret the device's output and provide accurate estimates of glucose concentration?

What is the user perception of comfort, safety, and practicality when the device is used in a routine hospital environment?

This study will not assign any interventions to participants; it is purely observational. The novel device is non-invasive, and its use will not interfere with standard clinical care. Measurements will be taken passively or concurrently with routine care procedures.

Participants will:

Continue to receive standard clinical care, including conventional monitoring of glucose, heart rate, and oxygen saturation.

Undergo additional measurements using the investigational device, which will be placed non-invasively on the skin (finger).

Answer a short usability questionnaire assessing their experience with the device, including any discomfort, perceived safety, or ease of use.

Data obtained from the device will be compared with routine clinical data from standard hospital devices (e.g., glucometers, pulse oximeters) to evaluate accuracy and reliability. No pharmacological, radiological, or invasive procedures will be involved.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18-75 years * Able to provide informed consent Exclusion Criteria: * Skin diseases or injuries on the fingers (e.g., psoriasis, open wounds, burns) * Tattoos on the fingers * Severe peripheral circulation disorders * Pregnancy * Presence of active implantable medical devices (e.g., pacemakers)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Endocrinology, Diabetology and Internal Medicine at the T. Marciniak Lower Silesian Specialist Hospital in Wrocław Wroclaw Lower Silesian Voivodeship

More Wrocław University of Science and Technology trials in Poland

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06973317 on ClinicalTrials.gov ↗ ← All trials in Poland