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临床试验/NCT07563491
NCT07563491已完成不适用

Comparison of Effectiveness in Patients of Gastroesophageal Reflux Disease Taking Esomeprazole Versus Vonoprazan.

Muhammad Aamir Latif1 个研究点 分布在 1 个国家目标入组 824 人开始时间: 2025年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
824
试验地点
1
主要终点
Sufficient relief

研究概览

简要总结

Local literature is deprived of data comparing the effectiveness of esomeprazole and vonoprazan in patients with gastroesophageal reflux disease (GERD). This study was planned with the objective of comparing the effectiveness of esomeprazole versus vonoprazan in patients diagnosed with GERD.

详细描述

Addressing the pressing need for an in-depth understanding and comparison of treatment options for the escalating prevalence of GERD, a condition significantly impacting patients' quality of life, is crucial. The study's results would not only provide local data, but also help doctors choose between esomeprazole and vonoprazan as the best treatment option. This would improve patient care and help doctors make better decisions, which would ultimately lead to better management of GERD and the overall health of patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any gender
  • Aged 18 to 65 years
  • Presenting with GERD

排除标准

  • Patients with hepatic, renal, respiratory, or cardiac disease accessed on history and medical records.
  • Any previous history of malignancy accessed from medical records.
  • Pregnancy and Lactation
  • Currently using histamine-2 receptor antagonists, antacids, gastrointestinal motility stimulants, and steroids.
  • History of drug allergy to proton pump Inhibitors (PPIs).

研究组 & 干预措施

Group-A

Experimental

Patients received a once-daily dose of 20 mg of esomeprazole after the evening meal for 4 weeks.

干预措施: Esomeprazole (Drug)

Group-B

Experimental

Patients received a once-daily dose of 20 mg of vonoprazan after the evening meal for 4 weeks.

干预措施: Vonoprazan (Drug)

结局指标

主要结局

Sufficient relief

时间窗: 4 weeks

The frequency of patients who achieved sufficient relief was noted.

次要结局

未报告次要终点

研究者

发起方
Muhammad Aamir Latif
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Muhammad Aamir Latif

Research Consultant

RESnTEC, Institute of Research

研究点 (1)

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