Skip to content

Clinical trial of D-psicose in patients with type 2 diabetes

Clinical trial of D-psicose in patients with type 2 diabetes - Clinical trial of D-psicose

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000035730
Enrollment
30
Registered
2019-01-31
Start date
2011-12-01
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

D-psicose is orally administered 15 g / day

Sponsors

kagawa university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Type 2 diabetes patients (HbA1c 6.5% or more) who can not obtain sufficient effect by any of the following treatments 1) Diet therapy or exercise therapy only 2) Pharmacotherapy in addition to diet therapy and exercise therapy

Exclusion criteria

Exclusion criteria: 1) Patients falling under D-psicose administration contraindications 2) Patients participating in other clinical trials 3) A pregnant woman, a maternity woman, a lactating woman or a woman having a possibility of pregnancy 4) Patients who have poor glycemic control with HbA1c> 8% 5) Patients who have severe renal dysfunction (serum creatinine value> 1.5 mg / dl) 6) Patients with other serious complications 7) Other patients judged inappropriate for judgment by other doctor's judgment

Design outcomes

Primary

MeasureTime frame
The change amount of HbA1c value at the 12th week after administration from the start of administration

Secondary

MeasureTime frame
Change in fasting blood glucose level or 2-hour postprandial blood glucose level and other blood test items

Countries

Japan

Contacts

Public Contactkoji murao

kagawa university Department of Endocrinology and Metabolism, Faculty of Medicine

labmed@med.kagawa-u.ac.jp+81878912230

Outcome results

None listed

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