跳至主要内容
临床试验/NL-OMON47484
NL-OMON47484已完成不适用

Adaptive Dose-Escalated Multi-modality Image-guided RadiothErapy (ADMIRE) for head and neck cancer by twice re-imaging, re-delineation and re-planning during the course of radiotherapy - ADMIRE

Antoni van Leeuwenhoek Ziekenhuis0 个研究点目标入组 20 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 64(—)

入选标准

  • Histologic biopsy confirmed squamous cell carcinoma of the oral cavity, HPV-negative oropharynx, hypopharynx or larynx
  • Scheduled for radiotherapy or radiotherapy with cisplatin or cetuximab

排除标准

  • Other neoplasms with metastases in the previous 3 years

研究者

发起方
Antoni van Leeuwenhoek Ziekenhuis

相似试验

招募中
3 期
Image-guided focal dose escalation in patients with primary prostate cancer treated with primary external beam hypofractionated radiation therapy (HypoFocal) – a prospective, multicenter, randomized phase III study.Prostate Cancer
DRKS00022915niversitätsklinikum Freiburg374
招募中
不适用
Functional imaging-guided radiotherapy dose escalation in rectal adenocarcinoma: a feasibility studyRectal cancerCancer - Bowel - Back passage (rectum) or large bowel (colon)
ACTRN12620000757910Dr Myo Min30
进行中(未招募)
不适用
An adaptive dose-ranging, multi-center, single-blind, double-dummy, active-controlled trial to determine the target dose of canakinumab (ACZ885) in the treatment of acute flares in gout patients who are refractory or contraindicated to NSAIDs and/or colchicine - H2255Acute gout (patients who are refractory or contraindicated to NSAIDs and/or colchicine)MedDRA version: 9.1Level: LLTClassification code 10018628Term: Gout acute
EUCTR2008-004666-61-GBovartis Pharma Services AG200
进行中(未招募)
不适用
An adaptive dose-ranging, multi-center, single-blind, double-dummy, active-controlled trial to determine the target dose of canakinumab (ACZ885) in the treatment of acute flares in gout patients who are refractory or contraindicated to NSAIDs and/or colchicine - H2255
EUCTR2008-004666-61-FIovartis Pharma Services AG200
进行中(未招募)
不适用
An adaptive dose-ranging, multi-center, single-blind, double-dummy, active-controlled trial to determine the target dose of canakinumab (ACZ885) in the treatment of acute flares in gout patients who are refractory or contraindicated to NSAIDs and/or colchicine
EUCTR2008-004666-61-FRovartis Pharma Services AG200