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Compares a glucose-monitoring device with blood tests in diabetes

Compares a device that measures glucose without blood samples to blood tests.

Plain-language title generated from the registry record
Registry title: The ELG Analysis of Glucose a Correlational to Blood Glucose Assay

Key facts

Where
Springdale, United StatesSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 25 to 65 with type 1 or type 2 diabetes. It compares a glucose device that needs no blood sample with blood tests.

Age
25 to 65 years
Sex
Men and women can join.
Disease stage
Diagnosed with type 1 or type 2 diabetes.
Earlier treatment
No other research study in the last 30 days. No blood transfusion or severe blood loss in the last 14 days.

Main reasons for not taking part

  • Taking drugs of abuse (illegal and/or prescription)
  • In another research study in the last 30 days
  • Blood transfusion or severe blood loss in the last 14 days
  • Sickle Cell Anemia

Read by machine on 12 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 25 and 65 years old?

Source: NCT05055804, who can take part

Where in United States

  • Rouse Family Medical ClinicSpringdale, United StatesNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
XP Technology, LLC
Trial code
NCT05055804
Record updated
16 January 2025
Original description
This study is an investigational study of the ELG medical device to monitor glucose blood level in diabetes mellitus Type 1 and 2 without blood samples in comparison to blood testing methods."Investigational" means the ELG medical device is subjected by the FDA (Food and Drug Administration) for premarket testing requirements. The purpose of this study is to collect data comparison values between ELG testing device to current blood testing methods.Read full original descriptionShow less

The ELG Analysis of Glucose a Correlational to Blood Glucose Assa

This study is an investigational study of the ELG medical device to monitor glucose blood level in diabetes mellitus Type 1 and 2 without blood samples in comparison to blood testing methods."Investigational" means the ELG medical device is subjected by the FDA (Food and Drug Administration) for premarket testing requirements. The purpose of this study is to collect data comparison values between ELG testing device to current blood testing methods.

Inclusion: Have been diagnosed with type 1 or 2 diabetes; Be 25 - 65 years of age; Male or female; Various ethnicities are desired; Must be available for 2 visits within a 2-4 week period and willing to spend up to 1-2 hours/visit; Must have daytime availability for visits; Able to have 1 venous blood draw \& up to 4 fingersticks for complete blood testing at each visit; Must be willing and able to fast (for at least 6 hours) prior to first visit.

Exclusion: Taking drugs of abuse (illegal and/or prescription); Have been in another research study in the last 30 days; Have had a blood transfusion or severe blood loss in the last 14 days; Have Sickle Cell Anemia.

ClinicalTrials.gov NCT05055804