Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

2 clinical studies listed.

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Blood Glucose Monitoring

Tundra lists 2 Blood Glucose Monitoring clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07256652

How Does YES Bar Affect Blood Glucose Levels?

Curious to see if there is a sweet treat that doesn't spike your blood sugar (avoiding the energy crash, inflammation, and weight gain)? This study uses the Abbott Lingo CGM to see how your blood glucose levels responds to YES Bar-an all natural, gluten-free, plant-based bar that tastes like dessert. You'll track your levels before and after eating it to see if it fits into your metabolic health. (iOS Only)

Gender: All

Updated: 2025-12-26

1 state

Blood Glucose Monitoring
NOT YET RECRUITING

NCT06973317

Self-Powered Photodetectors for Smarter Healthcare

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.

Gender: All

Ages: 18 Years - 75 Years

Updated: 2025-07-10

1 state

Blood Glucose Monitoring