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临床试验/EUCTR2012-001128-36-ES
EUCTR2012-001128-36-ES进行中(未招募)不适用

Integral care program with or without palliative chemotherapy in patients with advanced cancer: multicentre randomized clinical trial. - PAI (Programa de atención Integral)

Institut de Recerca HSCSP0 个研究点开始时间: 2012年6月25日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Men and women ? 18 years of age.
  • 2. Patients potentially eligible to receive a new chemotherapy treatment and whose clinical condition, according to the oncologist responsible, does not identify any therapeutic strategy clearly superior to another, in the light of available scientific evidence.
  • 3. Patients with advanced cancers that have been treated with chemotherapy but have not submitted a complete response to treatment or who, having presented, are now in a situation of recurrence or disease progression
  • 5. Patients who have previously completed a number of chemotherapies. Depending on the type of cancer will be considered:
  • ? Cancers of the digestive and gastrointestinal
  • ? Head and Neck Cancers
  • ? Cancer Bronchopulmonary
  • ? Urological Cancer
  • ? Gynecologic Cancer
  • ? Central Nervous System Cancer
  • 6. Patients with potential capacity to complete the study, and accept and sign the informed consent.
  • 7. Patients whose home is located less than 10 km from the hospitals participating in the study.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 200
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 22

排除标准

  • 1. Patients who are in course of any chemotherapy. Not be considered an exclusion criterion that the patient is enrolled in any other concomitant therapy (e.g., hormone or radiation therapy).
  • 2. Patients with contraindications to chemotherapy.
  • 3. Patients who refuse to enter into the clinical trial.

研究者

发起方
Institut de Recerca HSCSP

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