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临床试验/JPRN-jRCTs061230051
JPRN-jRCTs061230051招募中3 期

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

Tanito Masaki0 个研究点目标入组 24 人开始时间: 2023年8月21日最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 < 70age old(—)
性别
All

入选标准

  • 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.
  • 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.

排除标准

  • 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.

研究者

发起方
Tanito Masaki

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