跳至主要内容
临床试验/ACTRN12614000858695
ACTRN12614000858695终止2 期

A single arm, prospective Phase II study to evaluate the effect of Split-Course Pelvic Radiotherapy on bladder and bowel health related quality of life in patients with locally progressive, castrate resistant prostate cancer.

Radiation Oncology Services - Mater Centre0 个研究点目标入组 18 人开始时间: 2014年8月11日最近更新:
适应症

试验速览

阶段
2 期
状态
终止
发起方
入组人数
18

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
Male

入选标准

  • Aged 18 years or older
  • Has provided written Informed Consent for participation in this trial
  • Histological or cytologically confirmed prostate cancer or where diagnosis made on clinical factors, a PSA >100ug/L at diagnosis
  • Castrate resistant disease, as defined by a rising PSA despite castrate levels of testosterone <0.5 ug/L
  • Patient has symptoms attributable to local disease progression OR is asymptomatic with T3 or T4 disease but and felt to be at risk of symptomatic local progression (these patients to be included in analysis of secondary endpoints 1, 3 and 4)
  • An ECOG performance status score of 2 or less
  • Life expectancy at least 6 months
  • Available for follow up at least via a phone interview.
  • Radiotherapy can commence within 6 weeks of trial registration.
  • Is able to complete QOL assessments

排除标准

  • Previous radiotherapy to the pelvis
  • Bilateral hip replacement surgery
  • Cytotoxic chemotherapy within 4 weeks of the proposed start date for radiotherapy
  • Prior diagnosis of cancer within 5 years of current diagnosis with the exception of successfully treated non-melanoma skin cancer

研究者

发起方
Radiation Oncology Services - Mater Centre

相似试验

尚未招募
2 期
Addition of resveratrol copper with chemotherapy in gastric cancer patients
CTRI/2019/07/020289Tata Memorial Hospital
进行中(未招募)
1 期
A Phase II, open-label, single arm study to evaluate the safety, efficacy, and pharmacokinetics of twice daily midostaurin (PKC412) combined with standard chemotherapy and as a single agent post-consolidation therapy in children with untreated FLT3-mutated AMuntreated FLT3-mutated acute myeloid leukemiaMedDRA version: 21.0Level: LLTClassification code 10000886Term: Acute myeloid leukemiaSystem Organ Class: 100000004864
EUCTR2017-004830-28-DEovartis Pharma AG23
进行中(未招募)
1 期
A Phase II, open-label, single arm study to evaluate the safety, efficacy, and pharmacokinetics of twice daily midostaurin (PKC412) combined with standard chemotherapy and as a single agent post-consolidation therapy in children with untreated FLT3-mutated AMuntreated FLT3-mutated acute myeloid leukemiaMedDRA version: 21.0Level: LLTClassification code 10000886Term: Acute myeloid leukemiaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
EUCTR2017-004830-28-ATovartis Pharma AG23
进行中(未招募)
1 期
A Phase II, open-label, single arm study to evaluate the safety, efficacy, and pharmacokinetics of twice daily midostaurin (PKC412) combined with standard chemotherapy and as a single agent post-consolidation therapy in children with untreated FLT3-mutated AM
EUCTR2017-004830-28-ITOVARTIS PHARMA AG52
进行中(未招募)
1 期
A Phase II, open-label, single arm study to evaluate the safety, efficacy, and pharmacokinetics of twice daily midostaurin (PKC412) combined with standard chemotherapy and as a single agent post-consolidation therapy in children with untreated FLT3-mutated AMuntreated FLT3-mutated acute myeloid leukemiaMedDRA version: 21.0Level: LLTClassification code 10000886Term: Acute myeloid leukemiaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
EUCTR2017-004830-28-CZovartis Pharma AG23