跳至主要内容
临床试验/CTRI/2024/11/076826
CTRI/2024/11/076826尚未招募不适用

Pharmacoeconomic analysis to determine the relative costeffectiveness of drugs used for primary open angle glaucoma or ocular hypertension

未提供1 个研究点 分布在 1 个国家目标入组 123 人开始时间: 2024年11月26日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
123
试验地点
1
主要终点
Cost effectiveness analysis

研究概览

简要总结

Various treatment options available for glaucoma differ in terms of expense, effectiveness, and side effects. There is a need of designing a cost effective treatment especially for chronic illness requiring life-long medication which can be beneficial for patients, health care providers and the government. All treatment solutions must be prioritized and rationalised in light of the growing disparity between available health resources and therapeutic options. The primary concern of the economic analysis of glaucoma treatment should be on efficiency—that is, the benefits of the treatment relative to the expenses or sacrifices involved in achieving the goals. Clinical effectiveness alone is no longer sufficient. Given the significance of cost-effectiveness, the objective of this research is to assess the daily and annual costs of treating glaucoma with medications that are now available in India, as well as the cost-effectiveness analysis.

 Hypothesis: As varied treatment options of wide cost range for glaucoma treatment are available in Indian market, a more economically sustainable anti-glaucoma medication treatment protocol can be designed by conducting cost-effectiveness analysis of these drugs.

Research question: Given the long-term financial burden of glaucoma therapy, can a more economically viable treatment protocol be designed for glaucoma patients?

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Age of 18 years and above 2) either gender 3) newly detected case of POAG/OHT 4) Unilateral or bilateral POAG or OHT with IOP more than 21 mm Hg. 5) Patients with bilateral POAG will be treated for both eyes, but the eye with greater decrease in IOP will be considered as the study eye.

排除标准

  • Patients with closed anterior chamber angle or acute angle closure glaucoma 2) Any history of intraocular surgery within 6 months of study, 3) Ocular infection or inflammation 4) Established diagnosis of secondary glaucoma 5) Pregnant and lactating females 6) Patients taking any other medication affecting IOP.

结局指标

主要结局

Cost effectiveness analysis

时间窗: Cost effectiveness analysis | at 4 weeks

次要结局

  • Adverse reactions analysis(4 weeks)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Dr Rima Shah

AIIMS Rajkot

研究点 (1)

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