Neuroprotective Activity of Rasayana Formulation and Effect of Shigru Pallava Eye Drops on Intraocular Pressure as an Add-on Therapy Compared to the Standard of Care in Primary Open-Angle Glaucoma: Protocol for an Exploratory, Open-label, Two-arm Randomized Controlled Trial.

Q2 Pharmacology, Toxicology and Pharmaceutics
F1000Research Pub Date : 2025-04-22 eCollection Date: 2025-01-01 DOI:10.12688/f1000research.163722.1
Deenadayal Devarajan, Manjusha Rajagopala
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引用次数: 0

Abstract

Background: Primary open-angle glaucoma (POAG) is a major cause of irreversible blindness worldwide, characterized by progressive optic neuropathy and loss of retinal ganglion cells (RGCs). Although lowering intraocular pressure (IOP) remains the mainstay of glaucoma management, many patients continue to experience vision loss, underscoring the need for adjunctive neuroprotective approaches. In Ayurveda, Rasayana therapies are believed to slow degenerative processes. One such intervention is a Rasayana Formulation (RF) comprising three oral preparations; Rasayana Churna (RC), Saptamrita Lauha (SL), and Yashada Bhasma (YB). Additionally, topical Arka (distilled extract) of Shigru Pallava (SP) has been used traditionally for glaucoma and may have an IOP-lowering effect.

Methods: This is an open-label, two-arm, parallel-group randomized controlled trial with a 2:3 (control: intervention) allocation ratio. A total of 50 previously or newly diagnosed POAG patients (IOP < 30 mmHg) are planned for enrollment. The control group receives the conventional standard of care alone, whereas the intervention group receives standard care plus RF (2.5 g, taken orally twice daily) and SP eye drops (1 drop, four times daily), administered for 90 days with a further 90-day follow-up. Primary outcomes include changes in optic nerve function measured by visual field indices (mean deviation (MD), pattern standard deviation (PSD), visual field index (VFI)) and retinal nerve fiber layer (RNFL) thickness, while secondary outcomes include IOP changes.

Results: Participant recruitment and data collection are ongoing. Final outcomes will be disseminated in peer-reviewed journals.

Conclusions: If shown to be effective, the combined RF and SP eye drops could enhance neuroprotection and further control IOP in POAG, thereby addressing a significant need in current glaucoma therapy. This trial may provide a foundation for larger-scale investigations into integrative treatments for glaucoma management.

Trial registration: Clinical Trial Registry of India (CTRI) no. CTRI/2023/06/053681, dated 08.06.2023.Available from: https://trialsearch.who.int/Trial2.aspx?TrialID=CTRI/2023/06/053681 Protocol Version: 3.0, dated 05.01.2023.

与标准治疗相比,Rasayana配方的神经保护活性和Shigru Pallava滴眼液作为附加治疗对原发性开角型青光眼的眼压的影响:一项探索性、开放标签、两组随机对照试验的方案
背景:原发性开角型青光眼(POAG)是世界范围内不可逆性失明的主要原因,其特征是进行性视神经病变和视网膜神经节细胞(RGCs)的丧失。虽然降低眼压(IOP)仍然是青光眼治疗的主要方法,但许多患者仍然经历视力下降,这强调了辅助神经保护方法的必要性。在阿育吠陀,Rasayana疗法被认为可以减缓退化过程。其中一种干预措施是包含三种口服制剂的Rasayana制剂(RF);Rasayana Churna (RC), Saptamrita Lauha (SL)和Yashada Bhasma (YB)。此外,外用紫檀(SP)的Arka(蒸馏提取物)传统上用于青光眼,可能具有降低眼压的作用。方法:这是一项开放标签、双臂、平行组随机对照试验,分配比例为2:3(对照组:干预组)。计划纳入50例先前或新诊断的POAG患者(IOP < 30mmhg)。对照组接受常规标准护理,干预组接受标准护理加RF (2.5 g,每日口服2次)和SP滴眼液(1滴,每日4次),给药90天,随访90天。主要结局包括视神经功能的变化,以视野指数(平均偏差(MD)、模式标准差(PSD)、视野指数(VFI)和视网膜神经纤维层(RNFL)厚度测量,次要结局包括IOP的变化。结果:参与者招募和数据收集正在进行中。最终结果将在同行评议的期刊上发表。结论:RF + SP联合滴眼液可增强POAG患者的神经保护作用,进一步控制IOP,满足当前青光眼治疗的重要需求。该试验可能为青光眼综合治疗的大规模研究提供基础。试验注册:印度临床试验注册(CTRI)号。CTRI/2023/06/053681,日期为2023年6月8日。可从:https://trialsearch.who.int/Trial2.aspx?TrialID=CTRI/2023/06/053681协议版本:3.0,日期为05.01.2023。
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来源期刊
F1000Research
F1000Research Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.00
自引率
0.00%
发文量
1646
审稿时长
1 weeks
期刊介绍: F1000Research publishes articles and other research outputs reporting basic scientific, scholarly, translational and clinical research across the physical and life sciences, engineering, medicine, social sciences and humanities. F1000Research is a scholarly publication platform set up for the scientific, scholarly and medical research community; each article has at least one author who is a qualified researcher, scholar or clinician actively working in their speciality and who has made a key contribution to the article. Articles must be original (not duplications). All research is suitable irrespective of the perceived level of interest or novelty; we welcome confirmatory and negative results, as well as null studies. F1000Research publishes different type of research, including clinical trials, systematic reviews, software tools, method articles, and many others. Reviews and Opinion articles providing a balanced and comprehensive overview of the latest discoveries in a particular field, or presenting a personal perspective on recent developments, are also welcome. See the full list of article types we accept for more information.
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