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临床试验/NCT06469957
NCT06469957已完成不适用

Impact of Hospital Pharmacist on Drug Management in Patients With Bronchopulmonary Cancer Treated by Chemotherapy and/or Immunotherapy or Oral Targeted Therapy

Centre Hospitalier Régional d'Orléans2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年6月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
2
主要终点
Impact of hospital pharmacist (interview) on the number of unscheduled consultations/hospitalizations.

研究概览

简要总结

This is a prospective, non-interventional study to evaluate impact of hospital pharmacist on drug management in patients (only questionnaires) with bronchopulmonary cancer treated by Chemotherapy and/or Immunotherapy or Oral targeted therapy. The primary objective of the study is to evaluate the number of unscheduled consultations/hospitalizations during 6 months.

详细描述

Currently, several treatments can be used for bronchopulmonary cancers: targeted oral therapy (OCT), oral chemotherapy, iv chemotherapy, iv immunotherapy. These therapies are rather unknown to community pharmacy and induce several adverse effects and drug interactions. These treatments require collaboration between different professionals (community and hospital pharmacists) in order to allow follow up and security in patient supportive care.

In our context of shortage of care staff, with a polymedicated and elderly population, we would like to assess the impact of hospital pharmacist in the drug management for patient with bronchopulmonary cancers treated by these therapies.

Other French studies (Lille, Angers, Tours) involving hospital pharmacists were carried out and aimed to evaluate the number of pharmaceutical interventions carried out without assessing the impact on the patient. In addition, no study concerns the Center Val de Loire region.

The aim of the study is to impact of hospital pharmacist (interview) on the number of unscheduled consultations/hospitalizations.

This is a prospective, non-interventional study to evaluate impact of hospital pharmacist on drug management in patients with bronchopulmonary cancer. Participants will be included after being informed and after obtaining no opposition to participate. Data collection sheet will be performed by hospital pharmacist at inclusion. Participants will be treated according to standard of care for cancer treatment. An interview will be performed 1 month, 3 months and 6 months after inclusion between hospital pharmacist and participant to obtain information's on cancer treatments (questionnaires). These interviews will be performed by phone or when the patient comes to the hospital for a follow-up consultation as part of the treatment of his cancer (standard of care).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Male or female ≥ 18 years
  • Patient without cognitive impairments
  • Patient with bronchopulmonary cancer
  • Patient treated by chemotherapy, immunotherapy or oral targeted therapy

排除标准

  • Patient informed and opposed to participate
  • Language barrier and lack of translator
  • Patient under guardianship, curatorship or deprived of liberty
  • Pregnant or breastfeeding women
  • Participation in any drug clinical drug trials
  • Patient with no insurance

结局指标

主要结局

Impact of hospital pharmacist (interview) on the number of unscheduled consultations/hospitalizations.

时间窗: From enrolment to the end of the follow up phase (6 months)

Number of unscheduled consultations or hospitalizations during the follow up phase

次要结局

  • Impact of hospital pharmacist (interview) on cancelled consultations/hospitalizations rate(From enrolment to the end of the follow up phase (6 months))
  • Impact of hospital pharmacist (interview) on treatment observance (number of dispensation)(From enrolment to the end of the follow up phase (6 months))
  • Impact of hospital pharmacist (interview) on treatment observance (gap between dispensation)(From enrolment to the end of the follow up phase (6 months))
  • Impact of hospital pharmacist (interview) on adverse effects(From enrolment to the end of the follow up phase (6 months))
  • Impact of hospital pharmacist (interview) on adverse effects leading to interrupted or withdrawn treatment(From enrolment to the end of the follow up phase (6 months))
  • Impact of hospital pharmacist on pharmaceutical intervention(From enrolment to the end of the follow up phase (6 months))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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