Devarajan Deenadayal, Rajagopala Manjusha
Shalakya Tantra, All India Institute of Ayurveda, New Delhi, 110076, India.
F1000Res. 2025 Apr 22;14:454. doi: 10.12688/f1000research.163722.1. eCollection 2025.
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, 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.
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.
Participant recruitment and data collection are ongoing. Final outcomes will be disseminated in peer-reviewed journals.
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.
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 3.0, dated 05.01.2023.
原发性开角型青光眼(POAG)是全球不可逆性失明的主要原因,其特征为进行性视神经病变和视网膜神经节细胞(RGCs)丧失。尽管降低眼压(IOP)仍然是青光眼治疗的主要手段,但许多患者仍持续出现视力丧失,这凸显了辅助性神经保护方法的必要性。在阿育吠陀医学中,某些疗法被认为可以减缓退行性病变进程。其中一种干预措施是一种由三种口服制剂组成的回春配方(RF);回春散(RC)、七味铁屑丸(SL)和炉甘石煅(YB)。此外,传统上已将刺桐叶(SP)的外用蒸馏提取物(Arka)用于青光眼治疗,可能具有降低眼压的作用。
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)。计划招募总共50名既往或新诊断的POAG患者(眼压<30 mmHg)。对照组仅接受传统标准治疗,而干预组接受标准治疗加RF(2.5 g,每日口服两次)和SP眼药水(1滴,每日四次),持续给药90天,并进行为期90天的随访。主要结局包括通过视野指标(平均偏差(MD)、模式标准偏差(PSD)、视野指数(VFI))和视网膜神经纤维层(RNFL)厚度测量的视神经功能变化,次要结局包括眼压变化。
参与者招募和数据收集正在进行中。最终结果将在同行评审期刊上发表。
如果证明有效,联合使用RF和SP眼药水可增强POAG的神经保护作用并进一步控制眼压,从而满足当前青光眼治疗中的一项重大需求。该试验可能为青光眼综合治疗的大规模研究提供基础。
印度临床试验注册中心(CTRI)编号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获取,版本3.0,日期为2023年1月5日。