跳至主要内容
临床试验/NCT05634681
NCT05634681招募中不适用

Plan-of-the-day Radiotherapy for Patients With Locally Advanced Cervical Cancer - a Prospective Randomized Controlled Trial (the POD-protocol)

Oslo University Hospital1 个研究点 分布在 1 个国家目标入组 190 人开始时间: 2022年11月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
190
试验地点
1
主要终点
To investigate whether implementation of the plan of the day concept results in less gastro-intestinal toxicity.

研究概览

简要总结

The study objectives are to improve the treatment of LACC patients and to increase knowledge of the potential benefit of the plan-of-the-day concept on side effects during and after radiotherapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

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

入选标准

  • •Histologically confirmed cervical cancer eligible for definitve radiochemotherapy
  • •FIGO stage IB1-IVa
  • •Over 18 years
  • •Speaks and understands Norwegian or English.
  • •Histology: Squamous cell carcinoma, adenocarcinoma, adenosquamous carcinoma
  • •Ability to understand and fill in patient questionnaires, and willing to sign a written informed consent
  • •Large movers (LM), fundus movement ≥2,5 cm.

排除标准

  • •Evidence of distant metastasis. Suspicious paraaortic lymphnodes below the renal vessels is allowed if they are covered by the radiation field
  • •Patients with previous surgery for their cervical cancer
  • •Uncontrolled intercurrent somatic illness.
  • •Psychiatric illness /social situations limiting study compliance
  • •Prior radiotherapy to the pelvis
  • •Patients who are pregnant or breastfeeding is excluded due to risk of teratogenic and abortifacient effects of radiotherapy and cisplatin, and the potential risk of adverse effect of nursing infants
  • •Patients under current treatment for other invasive s except non-melanoma skin cancers
  • •Nephrostomy
  • •Patients with inflammatory bowel disease

研究组 & 干预措施

Control arm

Active Comparator

干预措施: Standard plan (Radiation)

Intervention arm

Experimental

干预措施: Plan of the day (Radiation)

结局指标

主要结局

To investigate whether implementation of the plan of the day concept results in less gastro-intestinal toxicity.

时间窗: 5 weeks

To compare the change in patient reported acute diarrhea from baseline to week 4 from start of the treatment and to the end of external radiotherapy. Item 17 in EORTC QLQ-C30

次要结局

未报告次要终点

研究者

发起方
Oslo University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kjersti Bruheim

MD PhD

Oslo University Hospital

研究点 (1)

Loading locations...

相似试验