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An exploratory study to examine the health benefits of the continuous drink of olive tea: a randomized, parallel group, controlled trial.

An exploratory study to examine the health benefits of the continuous drink of olive tea: a randomized, parallel group, controlled trial. - Continuous drink study of olive tea

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000020321
Enrollment
40
Registered
2015-12-24
Start date
2016-01-30
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 subjects

Interventions

Olive tea(1L/d*12 weeks) Green tea(1L/d*12 weeks)

Sponsors

Course of clinical research and regional innovation donated by the Japan Agriculture Ibaraki Public Welfare Federation Fuculty of Medicine University of Tsukuba
Lead Sponsor
Yamahisa Co.Ltd University of Tsukuba, Faculty of Life and enviromental sciences
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Aged 40 -70 years. 2)LDL-cholesterol not less than 120 mg/dL, under 160 mg/dL 3)Capable of giving informed consent

Exclusion criteria

Exclusion criteria: 1)Body mass index not less than 30.0 kg/cm2 2)Fasting blood glucose not less than 126 mg/dL 3)HbA1c not less than 6.5% 4)Subjects who are received pharmacotherapy for alimentary disease 5)No enrollment in another interventional study 6)Subjects who were recognized unsuitable for this study by the Investigator.

Design outcomes

Primary

MeasureTime frame
Lipid metabolic indicator after 12-week intervention

Secondary

MeasureTime frame
1.Body weight, Abdominal circumference 2.Blood pressure 3.Glucose metabolic indicator 4.Hepatic and renal function indicator 5.Bone turnover marker

Countries

Japan

Contacts

Public ContactKoichi Hashimoto

University of Tsukuba, Faculty of Medicene Clinical research and regional innovation donated by the JA Ibaraki Public Welfare Federation

koichi.hashimoto@md.tsukuba.ac.jp029-853-3064

Outcome results

None listed

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