Blood glucose performance test

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN11668805

Enrollment

Registered

2015-01-27

Start date

2014-10-29

Completion date

Unknown

Last updated

2020-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Nutritional, Metabolic, Endocrine Diabetes mellitus

Interventions

Either: Venepuncture will be performed and venous whole blood from the subject will be tested on the blood glucose monitoring system, the HemoCue analyser and the YSI analyser as whole

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Subjects has diabetes 2. Subject is willing to provide a whole blood sample for analysis using: 2.1. The blood glucose monitoring systems 2.2. HemoCue analyser 2.3. YSI analyser 3. The subject is able to understand the patient information sheet and sign the informed consent form prior to any clinical investigation plan directed activity

Exclusion criteria

Exclusion criteria: 1. Subject under 16 years of age 2. Subject is unwilling or unable to give consent for a blood sample to be collected

Design outcomes

Primary

Measure	Time frame
The accuracy of the blood glucose monitoring system compared to the YSI analyser using fingerstick capillary or venous whole blood samples	—

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026