Clinical Assessment of Preventive Strategies for Chemotherapy Induced Nausea Vomiting in Cancer Patients at a Tertiary Care Teaching Hospital: A Prospective Study
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
Dr Manjula G
KLE College of Pharmacy, Belagavi
