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临床试验/CTRI/2025/10/096586
CTRI/2025/10/096586尚未招募不适用

Clinical Assessment of Preventive Strategies for Chemotherapy Induced Nausea Vomiting in Cancer Patients at a Tertiary Care Teaching Hospital: A Prospective Study

KLE College of Pharmacy, Belagavi1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2025年11月10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
150
试验地点
1
主要终点
Evaluate the effectiveness of preventive strategies for chemotherapy induced nausea vomiting.

研究概览

简要总结

This is Prospective Study, where we include patients of cancer diagnosis and undergoing chemotherapy as treatment with histological/pathological confirmation and experiencing chemotherapy-induced nausea and vomiting and exclude cancer patient who are not undergoing any chemotherapy treatment but are taking other standard treatment. In this study we aim to assess the anti-emetics used to prevent chemotherapy-induced nausea and vomiting and factors associated with increased risk of chemotherapy induced nausea and vomiting. We also aim to determine the impact of chemotherapy-induced nausea and vomiting (CINV) on the quality of life of cancer patients and to evaluate the effectiveness of clinical pharmacist–led interventions, including patient information leaflets, educational videos, mobile applications, and individualized counselling, in improving patient quality of life.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

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

入选标准

  • Patients above 18yrs of both the gender.
  • Patients with a histological / pathological confirmation of cancer diagnosis.
  • Patients undergoing chemotherapy.

排除标准

  • Vulnerable patients (pregnant women, lactating women, disabled people).
  • Patients who are not on chemotherapy.
  • Patients who are not willing to participate in research.

结局指标

主要结局

Evaluate the effectiveness of preventive strategies for chemotherapy induced nausea vomiting.

时间窗: 1 week, 2 weeks and 3 weeks

Decreased incidence and severity of chemotherapy induced nausea and vomiting and Clinical pharmacist interventional tools to reduce CINV-related complications and improved patient quality of life.

时间窗: 1 week, 2 weeks and 3 weeks

次要结局

未报告次要终点

研究者

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

Dr Manjula G

KLE College of Pharmacy, Belagavi

研究点 (1)

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