The Effect of Hyperbaric Oxygen Treatment in Patients With Osteoradionecrosis.
NCT ID: NCT04934644
Last Updated: 2021-06-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
120 participants
INTERVENTIONAL
2019-03-19
2024-03-19
Brief Summary
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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.
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Detailed Description
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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.
Baseline visit will include clinical examination by an oral and maxillofacial surgeon and quality of life questionnaires developed and validated for head-and-neck cancer patients (EORTC QLQ C30 and H\&N35). The patients in the HBO group will also be examined by a doctor at the hyperbaric unit. Follow-up will be performed every third month during the first year. In total the patients will be followed for a period of four years, every sixth months the second and third year and then on a yearly basis from the third year and on if no need for more frequent controls exist. The follow-up will include clinical examination by an oral and maxillofacial surgeon, radiographies including CT-scan and quality of life questionnaires. This is according to established care program. Blood samples, and if the patient undergoes surgery, tissue samples, will also be collected to look at biomarkers for inflammation and bone turnover.
Primary end-point of the study is changes in the bone as well as the soft tissue surrounding the necrotic bone. Secondary end-points are improvements regarding pain, infection, mouth-opening capacity and quality of life scorings.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Hyperbaric oxygen treatment
30 HBO treatments and standard care. If surgery is needed an additional 10 HBO treatments postoperative.
Hyperbaric oxygen treatment
Hyperbaric oxygen treatment 90 min from start to start of decompression. The chamber is pressurized to 2,4 ATA and the patients will be breathing 100% oxygen. Treatments will be given once daily, five days a week (no treatments on weekends and holidays).
Control
Standard care. Surgery if needed.
No interventions assigned to this group
Interventions
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Hyperbaric oxygen treatment
Hyperbaric oxygen treatment 90 min from start to start of decompression. The chamber is pressurized to 2,4 ATA and the patients will be breathing 100% oxygen. Treatments will be given once daily, five days a week (no treatments on weekends and holidays).
Eligibility Criteria
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Inclusion Criteria
* 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 0-3.
* Ability to understand Swedish speech and writing.
* Received oral and written information about the study and given consent to participate in writing.
Exclusion Criteria
* 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 4.
* 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.
18 Years
ALL
No
Sponsors
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Göteborg University
OTHER
Responsible Party
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Principal Investigators
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Göran Kjeller, Docent
Role: STUDY_DIRECTOR
Department of oral and maxillofacial surgery, Institute of odontology, Sahlgrenska Academy, GU
Locations
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Department of oral and maxillofacial surgery, Institute of odontology, Sahlgrenska Academy, University of Gothenburg
Gothenburg, Göteborg, Sweden
Department of Oral and Maxillofacial Surgery, The University Hospital of Skåne
Lund, Skåne County, Sweden
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ORN
Identifier Type: -
Identifier Source: org_study_id
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