Traditional Chinese Herbal Medicine Buyang Huanwu Decoction on Visual Acuity and Visual Field in Patients With Normal Tension Glaucoma:a Double-blind, Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 60
- 主要终点
- Changes in visual acuity
研究概览
简要总结
The goal of this clinical trial is to test Buyang Huanwu Decoction in normal intra-ocular pressure glaucoma. The main question to answer is: the effect of Buyang Huanwu Decoction and its safety in patients with normal intra-ocular pressure glaucoma.
Participants will take 3 grams of Buyang Huanwu Decoction or placebo for 12 weeks.
Researchers will compare treatment group and placebo group to see if the visual acuity, visual field would be improved.
详细描述
There is currently no active and effective treatment for normal intra-ocular pressure glaucoma, and glaucoma patients often affect the optic nerve and cause visual acuity and visual field damage. Studies have found that glaucoma patients have less blood flow to the optic nerve, retina and choroid than normal people. Buyang Huanwu Decoction has the functions of invigorating qi, promoting blood circulation and dredging collaterals, and is often used in the treatment of stroke. Therefore, the purpose of this study is to investigate the effect of Buyang Huanwu Decoction on visual acuity, visual field and its safety in patients with normal intra-ocular pressure glaucoma. This study is designed as a randomized, double-blind, controlled clinical trial. A total of 60 subjects with normal intra-ocular pressure glaucoma were randomly divided into: 1) treatment group (30 subjects), oral administration of Buyang Huanwu Decoction (3 grams), two times in a day after breakfast and dinner, for 12 consecutive weeks; 2) control group (30 subjects), the same method as the treatment group, but taking Buyang Huanwu Decoction placebo (90% starch and 10% Buyang Huanwu Decoction). Primary outcome was changes in visual acuity, visual field, and optic nerve fiber layer, and secondary outcome was changes in quality of life scale scores.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 75 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosis of normal tension glaucoma for at least 3 months.
- •Using less than 1 medicine for glaucoma.
- •Without any eye disease other than normal tension glaucoma.
- •Writing the Informed Consent Form by themselves.
排除标准
- •With other chronic diseases, such as diabetes, hypertension, cancer.
- •With polypharmacy.
- •Had glaucoma surgery or myopia laser surgery before the study.
- •With mental disease and could not finish the study.
- •Allergic to Buyang Huanwu Decoction.
- •Pregnancy or lactation.
结局指标
主要结局
Changes in visual acuity
时间窗: 12 weeks
The difference of visual acuity between study baseline and the 12 weeks of intervention.
次要结局
未报告次要终点
研究者
Ching-Liang Hsieh
Physician
China Medical University Hospital
