Clinical trial to assess the effect of pinitol containing complex on postprandial blood glucose level.

Clinical trial to assess the effect of pinitol containing complex on postprandial blood glucose level. - Effect of pinitol on postprandial blood glucose level

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000023726

Enrollment

Registered

2016-08-26

Start date

2016-08-29

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

Healthy subject

Interventions

Sigle oral intake of pinitol containing complex Single oral intake of placebo

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.Healthy person aged from 18 to 25 y. 2.Non-athlete

Exclusion criteria

Exclusion criteria: 1. Subjects who is prescribed drug. 2. Subject who is or was with significant cardiovascular, hepatic, renal, pulmonary or metabolic disease. 3. Subjects who has allergy to the investigational dietary supplement ingredient. 4. Subjects who is participating or participated in a clinical research trial that affects glucose metabolism within 3 months.

Design outcomes

Primary

Measure	Time frame
Postprandial blood glucose level upto 2 hours after intake	—

Countries

Japan

Contacts

Public ContactYoshio Suzuki

Juntendo University Graduate School of Health and Sports Science

yssuzuki@juntendo.ac.jp+81-476-98-1001

Outcome results

None listed

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