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临床试验/CTRI/2025/07/090954
CTRI/2025/07/090954招募中不适用

Pharmaceutical Care impact on Health-Related Quality of Life (HRQoL) and Pharmacoeconomical Burden on COVID-Recovered Diabetic Patients with Comorbid Conditions

未提供1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2025年7月21日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
500
试验地点
1
主要终点
Improving of Health related quality of life

研究概览

简要总结

The worldwide commonness of diabetes is supposed to reach 10.5% (536.6 million individuals) by 2021, proposing a clinical emergency. Overseeing individuals with diabetes with comorbidities and those without COVID-19 overburdens the personal satisfaction and economy. To address this, medical care experts with clinical mastery have been attempting to foster a more extensive job in the therapy of diabetes. In spite of the fact that there is proof that drug treatment further develops glucose control, little is had some significant awareness of its impacts on human results, for example, wellbeing related personal satisfaction (HRQoL). The ebb and flow study incorporates a writing search in data sets, for example, IDF, CINAHL, Medline, Embase, Pubmed and worldwide articles by September 2021, alongside the extent of diabetes pharmacological treatment. For diabetics. Until this point in time, a couple of distributions have been distributed that show the pharmacological advantage of pharmacotherapy. There is no information to help guarantees that PCs have any sure monetary effect. This article surveys distributed examinations on the monetary investigation of medication organization to increment drug worth and supports the case that drug organization assists a PC with diminishing the monetary weight of patient downfall. locally by decreasing medication related dreariness and mortality.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • 1.Aged greater than 18 years 2.History of confirmed COVID-19 recovery 3.Diagnosed with Type 2 Diabetes Mellitus 4.At least one comorbid condition On pharmacologic treatment for diabetes and comorbidities 5.Able and willing to provide written informed consent.

排除标准

  • 1.Type 1 Diabetes Mellitus or gestational diabetes 2.Patients with cognitive impairment or severe psychiatric illness 3.Patients receiving investigational drugs or enrolled in other clinical trials 4.Pregnant or lactating women 5.Patients unwilling to participate in follow-up.

结局指标

主要结局

Improving of Health related quality of life

时间窗: 1.Baseline (T0): At enrollment | 2.3 months(T1):After Pharmaceutical care intervention period | 3.6 Months(T2): Long term follow up

次要结局

  • Pharmaco economic burden (Direct medical cost, Indirect Medical cost)(1.Base line:(T0))
  • Drug Related problems(Continuous monitoring, summarized at 3 & 6 months)

研究者

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

Sadanandam Akari

Malla Reddy Institute of Pharmacy

研究点 (1)

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