Investigation and Examination of the Usability of the Soflet Blood Collection Device and Soflet Needles

Investigation and Examination of the Usability of the Soflet Blood Collection Device and Soflet Needles - Investigation and Examination of the Usability of the Soflet Blood Collection Device and Soflet Needles

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000055870

Enrollment

Registered

2024-10-18

Start date

2024-04-07

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Diabetes

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria will be included in this study. 1) Diabetic patients aged 20 and over 2) Those who currently using the Gentlet blood glucose measurement puncture device and Gentlet needles, who have consented to switch to Soflet and Soflet needles 3) Those who have provided consent to participate in the study

Exclusion criteria

Exclusion criteria: Patients will be excluded from this study if they meet any of the following criteria: 1)Those who diagnosed with clear cognitive impairment, such as dementia or mild cognitive impairment (MCI) 2) Those whos with a mental illness 3) Those who currently participating in another study

Design outcomes

Primary

Measure	Time frame
usability of the device	—

Secondary

Measure	Time frame
Awareness regarding self-blood glucose measurement	—

Countries

Japan

Contacts

Public ContactKatunori Suzuki

Niigata Diabetes Clinic N/A

katsu-s@niigata-diabetes.jp025-370-1024

Outcome results