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临床试验/CTRI/2025/10/095714
CTRI/2025/10/095714尚未招募不适用

Assessment of Medication Errors and Drug-Drug Interactions among Cardiovascular Disease Patients: A Clinical Pharmacist Perspective.

KLE College of Pharmacy1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2025年10月20日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
160
试验地点
1
主要终点
Identification of medication errors and drug-drug interactions

研究概览

简要总结

Cardiovascular diseases (CVDs) are the leading cause of global mortality, with India reporting higher CVD-related death rates than the global average. The management of CVD often involves multiple medications, increasing the risk of medication errors (MEs) and drug-drug interactions (DDIs), which may lead to adverse drug reactions (ADRs), prolonged hospital stays, and higher healthcare costs. This prospective observational study aims to assess the incidence, types, and causes of medication errors and clinically significant DDIs among cardiovascular patients. It also seeks to evaluate the impact of clinical pharmacist interventions in identifying, preventing, and minimizing such medication-related problems. The study will be conducted in the Departments of Cardiology and General Medicine at KLE’s Dr. Prabhakar Kore Hospital and Medical Research Centre, Belagavi, involving 160 patients. Data will be collected using validated tools such as the ASHP scale for medication errors, Micromedex for DDIs, and WHO-UMC and Hartwig & Siegel scales for ADR assessment. Statistical analysis will determine the effectiveness of pharmacist interventions in improving medication safety and patient outcomes. The findings are expected to highlight the crucial role of clinical pharmacists in ensuring safer pharmacotherapy for cardiovascular patients.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients with cardiovascular patients with or without comorbidities
  • Both male and female patients of IPD and OPD of more than 18 years of age to 70 years of age.
  • 3.Patients who are willing to Participate.

排除标准

  • Pregnant and lactating women
  • Patients who have incomplete medication records or do not have the clinical or laboratory data needed for evaluation.

结局指标

主要结局

Identification of medication errors and drug-drug interactions

时间窗: Baseline and 8 weeks

次要结局

未报告次要终点

研究者

发起方
KLE College of Pharmacy
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Mandati Santhosh Reddy

KLE College of Pharmacy, Belagavi

研究点 (1)

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