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临床试验/NCT04934644
NCT04934644Unknown不适用

The Effect of Hyperbaric Oxygen Treatment in Patients With Osteoradionecrosis. A Prospective Multicenter Study.

Göteborg University4 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2019年3月19日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
120
试验地点
4
主要终点
SH-index

研究概览

简要总结

Osteoradionecrosis (ORN) is a severe delayed radiation-induced injury that can occur in patients whom have been subjected to radiotherapy for head and neck cancer. Hyperbaric oxygen treatment (HBO) is one treatment option. In Sweden it is used in some locations in combination to standard treatment which includes for example antibiotics, pain medication and surgery. There is still not sufficient evidence that this treatment is effective in this group of patients.

The primary aim of this study will be to evaluate HBO as a treatment for osteoradionecrosis in terms of slowing the progression of the disease, or at the best, cure the disease.

详细描述

Radiotherapy (RT) is frequently used for treatment of head and neck cancer, in combination with surgery and chemotherapy. Although RT can improve the survival rate among head and neck-cancer patients, it has negative effects on the healthy tissue surrounding the tumour. Osteoradionecrosis (ORN) is a severe delayed radiation-induced injury that can occur in patients whom have been subjected to RT for head and neck cancer. ORN can occur within months to several years after radiotherapy. Symptoms can include pain, dysesthesia, halitosis (bad breath) exposed necrotic bone, infection, orocutaneous fistula and pathologic fractures. The mandible is the most common site affected by ORN, but other bones can be affected as well. ORN has earlier been treated with long-term antibiotics and surgery. Today the treatment is multidisciplinary and also includes local wound care, hyperbaric oxygen (HBO) and new medications for example Pentoxifylline, a vasodilator that also inhibits fibrosis, Tocopherol (Vitamin E), that reduces damage by free radicals, and Clodronate, a bisphosphonate that inhibits bone resorption.

Hyperbaric oxygen treatment (HBO) is an intervention in which the individual breathes near 100% oxygen intermittently while inside a hyperbaric chamber that is pressurized to above sea level pressure. By increasing the inspired partial pressure of oxygen (PO₂), with an increased O₂ fraction inspired and increased pressure, the amount of oxygen in blood can be increased. This also increases the distance that oxygen can diffuse from the capillaries into the tissues. HBO increase production of reactive oxygen and nitrogen species. This leads to neovascularisation by two processes: blood vessel growth by local endothelial cells (angiogenesis) and recruitment and differentiation of stem cells to form vessels "de novo" (vasculogenesis). HBO has also been shown to stimulate fibroblast proliferation and enhances collagen synthesis.

The primary aim of this study will be to evaluate HBO as a treatment for osteoradionecrosis in terms of slowing the progression of the disease, or at the best, cure the disease. As secondary aims for this study, the effect of HBO on pain, infection, mouth-opening capacity and quality of life will be evaluated.

The study will be a prospective study with matched controls evaluating the effect of HBO in comparison to standard care in patients with ORN stage 1-2b according to classification of Kagan and Schwartz. A total of 60 patients in each group will be included, which should be sufficient for statistical significance according to power calculations.

The patients will be enrolled into two groups. The first group of patients will receive HBO treatment. The treatment will be given in a multi or monoplace chamber pressurized to 2,4-2,5 ATA, 90 minutes from start to decompression, and the patients will be breathing 100 % oxygen. Treatment will be given once daily, five days a week. All patients will receive 30 treatments and if surgery is needed the patient will receive an additional 10 treatments postoperatively. All according to local routines for treatment of ORN with HBO. The control group will consist of a group of patients with the same diagnosis and same stage of ORN. These will be patients from a maxillofacial unit in Sweden not using HBO treatment or patients who decline the treatment. The controls will be matched based on sex, age, tumour-stage and RT. These patients will be treated with standard care and be subjected to surgery if needed.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • Osteoradionecrosis in the head and neck area (Stage 1-2b according to the classification by Schwartz and Kagan)
  • Previous radiation with or without chemotherapy of a histologically verified primary tumor in the head and neck area.
  • Patient free of tumor.
  • Autonomous patient.
  • Age ≥18 years old.
  • WHO performance status 0-
  • Ability to understand Swedish speech and writing.
  • Received oral and written information about the study and given consent to participate in writing.

排除标准

  • Contraindications against HBO.
  • Participation in other ongoing study on osteoradionecrosis.
  • Pregnancy or planned pregnancy.
  • Woman in fertile age without effective contraceptive method.
  • Alcohol or drug abuse.
  • WHO performance status
  • Suspicion of recurrent tumor.
  • Mental health disorder or other condition which makes the patient unable to follow study protocol.
  • Not able to give informed concent.
  • Previous HBO.

结局指标

主要结局

SH-index

时间窗: 1-4 years

Assessment of healing of soft and hard tissue using SH-index S0H0-S1H3, where lower scores are a better outcome and higher scores are worse. The classification is based on clinical examination of the soft tissue (S) and radiographies of the hard tissue (H).

次要结局

  • Secretion of saliva(1-4 years)
  • Mouth opening capacity(1-4)
  • Infection(1-4 years)
  • Change in stage of osteoradionecrosis(1-4 years)
  • Transcutaneous perfusion measurement(1-4 years)
  • Perceived pain(1-4 years)
  • Alkaline phosphatase(1-4 years)
  • Perceived quality of life(1-4 years)

研究者

发起方
Göteborg University
申办方类型
Other
责任方
Sponsor

研究点 (4)

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