Skip to content

Questionnaire survey on the use of the OneDrawTM automated blood collection and storage device in patients with type 2 diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1032230486
Enrollment
30
Registered
2023-12-03
Start date
2023-10-16
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

Type 2 diabetes

Interventions

None listed

Sponsors

Seiji Hori
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria will be considered. 1) Age 18 years or older on the date of consent, regardless of gender 2) Outpatients with mild to moderate type 2 diabetes whose condition is stable 3) Patients who are able to adhere to medication adherence and diet and exercise regimen as directed 4) Patients with HbA1c less than 8.0% on the last 2 diabetes examinations prior to obtaining consent 5) Patients who have not changed their diabetes medications since the two previous visits at the time of obtaining consent and have no plans to do so until the end of this study 6) Patients who have received a thorough explanation of their participation in this study, and who have given written consent of their own free will based on sufficient understanding

Exclusion criteria

Exclusion criteria: Patients who violate the following criteria will be excluded from this study. 1) Patients with type I diabetes mellitus 2) Patients on insulin therapy 3) Patients who may exhibit severe ketosis, diabetic coma or pre-comatose state during study participation 4) Patients with unstable HbA1c levels 5) Patients with restrictions on diet and exercise due to other diseases or complications 6) Patients who are pregnant, lactating, may be pregnant, or are planning to become pregnant 7) Patients with impaired hemostatic function due to bleeding disorder or medication, or with shock or allergy 8) Other patients deemed by the physician to be ineligible for participation

Design outcomes

Primary

MeasureTime frame
Results of a survey on the use of the OneDra for patients with type 2 diabetes

Contacts

Public ContactHashimoto Masaki

Sumitomo Pharma Co., Ltd.

fbo_ir@sumitomo-pharma.co.jp+81-3-5205-3720

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026