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Clinical trial for effects of French maritime pine bark/bilberry fruit extracts on intraocular pressure for primary open angle glaucoma

Clinical trial for effects of French maritime pine bark/bilberry fruit extracts on intraocular pressure for primary open angle glaucoma

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs061230051
Enrollment
24
Registered
2023-08-21
Start date
2023-08-21
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

Primary open-angle glaucoma or ocular hypertension

Interventions

Participants are randomly assigned 1:1 to GP or PG group. GP group: take French maritime pine bark/bilberry fruit extracts for 8 weeks, followed by placebo for 8 weeks. PG group: take placebo for 8 we

Sponsors

Tanito Masaki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Primary open-angle glaucoma including juvenile open-angle glaucoma and normal tension glaucoma or ocular hypertension in one or both eyes. 2) Glaucoma progression and ocular hypertension are controlled with no medication or three or fewer medications (in the case of combination drugs, no more than five active ingredients). 3) No need for eye surgery, including glaucoma, within the next 12 months in either eye. 4) At least one eye has an intraocular pressure of 15 mmHg or greater by Goldmann applanation tonometer under the use of glaucoma medication. 5) Self-measurement of intraocular pressure and blood pressure is possible. 6) Written informed consent.

Exclusion criteria

Exclusion criteria: 1) Severe systemic illness. 2) Secondary glaucoma. 3) Other eye diseases leading to blindness, except glaucoma and mild cataracts. 4) Hepatic, renal, and cardiac disorders affecting assessment. 5) May cause allergic reactions to the test food. 6) May cause severe allergic reactions to other foods and medicines. 7) Continuous intake habits of antioxidant advocacy supplements (pine bark extract, bilberry, blackcurrant, lutein, astaxanthin, vitamin C, and vitamin E) in the 6 months before enrolment or planned to do so during the study period. 8) Lifestyle changes may be made during the study period (e.g. extended travel, change of diet). 9) Pregnant, lactating, or possibly pregnant. 10) Participation in another human clinical trial at the time of consent.

Design outcomes

Primary

MeasureTime frame
Intraocular pressure by Goldmann tonometer

Secondary

MeasureTime frame
Intraocular pressure by self-measurement, Blood pressure and Pulse by self-measurement, Blood oxidative stress markers, Carotenoids, Advanced Glycation End Products, Autonomic balance, Adverse events

Contacts

Public ContactMasaki Tanito

Shimane University Hospital

mtanito@med.shimane-u.ac.jp+81-853-20-2284

Outcome results

None listed

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