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The Effect of Hyperbaric Oxygen Treatment in Patients With Osteoradionecrosis. (ORN)

Primary Purpose

Osteoradionecrosis

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Hyperbaric oxygen treatment
Sponsored by
Göteborg University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoradionecrosis focused on measuring Osteoradionecrosis, Radiation injuries, Hyperbaric oxygenation, Hyperbaric oxygen treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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 0-3.
  • Ability to understand Swedish speech and writing.
  • Received oral and written information about the study and given consent to participate in writing.

Exclusion Criteria:

  • 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 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.

Sites / Locations

  • Department of oral and maxillofacial surgery, Institute of odontology, Sahlgrenska Academy, University of GothenburgRecruiting
  • Department of Oral and Maxillofacial Surgery, The University Hospital of Skåne

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Hyperbaric oxygen treatment

Control

Arm Description

30 HBO treatments and standard care. If surgery is needed an additional 10 HBO treatments postoperative.

Standard care. Surgery if needed.

Outcomes

Primary Outcome Measures

SH-index
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).

Secondary Outcome Measures

Change in stage of osteoradionecrosis
Schwartz and Kagan 1a-3b, where 1 is a better outcome and 3b is worse.
Infection
3-grade scale
Transcutaneous perfusion measurement
Perfusion of blood in the affected area
Perceived pain
Visual Analog Scale (VAS) 0-10, where 0 is a better outcome an 10 is worse.
Mouth opening capacity
mm
Secretion of saliva
ml/min
Perceived quality of life
EORTC (European organisation for research and treatment of cancer) quality of life questionnaire (QLQ C-30). A system for evaluating quality of life in cancer patients. Score 0-100, where a higher value is a higher quality of life.
Perceived quality of life
EORTC (European organisation for research and treatment of cancer) quality of life questionnaire (QLQ H&N35). A system for evaluating quality of life in patients with head and neck cancer. Score 0-100, where a higher value means more symptoms.
Alkaline phosphatase
An increased value indicates an increase in bone metabolism

Full Information

First Posted
May 17, 2021
Last Updated
June 14, 2021
Sponsor
Göteborg University
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1. Study Identification

Unique Protocol Identification Number
NCT04934644
Brief Title
The Effect of Hyperbaric Oxygen Treatment in Patients With Osteoradionecrosis.
Acronym
ORN
Official Title
The Effect of Hyperbaric Oxygen Treatment in Patients With Osteoradionecrosis. A Prospective Multicenter Study.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Recruiting
Study Start Date
March 19, 2019 (Actual)
Primary Completion Date
March 19, 2024 (Anticipated)
Study Completion Date
March 19, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Göteborg University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoradionecrosis
Keywords
Osteoradionecrosis, Radiation injuries, Hyperbaric oxygenation, Hyperbaric oxygen treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hyperbaric oxygen treatment
Arm Type
Experimental
Arm Description
30 HBO treatments and standard care. If surgery is needed an additional 10 HBO treatments postoperative.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Standard care. Surgery if needed.
Intervention Type
Procedure
Intervention Name(s)
Hyperbaric oxygen treatment
Intervention Description
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).
Primary Outcome Measure Information:
Title
SH-index
Description
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).
Time Frame
1-4 years
Secondary Outcome Measure Information:
Title
Change in stage of osteoradionecrosis
Description
Schwartz and Kagan 1a-3b, where 1 is a better outcome and 3b is worse.
Time Frame
1-4 years
Title
Infection
Description
3-grade scale
Time Frame
1-4 years
Title
Transcutaneous perfusion measurement
Description
Perfusion of blood in the affected area
Time Frame
1-4 years
Title
Perceived pain
Description
Visual Analog Scale (VAS) 0-10, where 0 is a better outcome an 10 is worse.
Time Frame
1-4 years
Title
Mouth opening capacity
Description
mm
Time Frame
1-4
Title
Secretion of saliva
Description
ml/min
Time Frame
1-4 years
Title
Perceived quality of life
Description
EORTC (European organisation for research and treatment of cancer) quality of life questionnaire (QLQ C-30). A system for evaluating quality of life in cancer patients. Score 0-100, where a higher value is a higher quality of life.
Time Frame
1-4 years
Title
Perceived quality of life
Description
EORTC (European organisation for research and treatment of cancer) quality of life questionnaire (QLQ H&N35). A system for evaluating quality of life in patients with head and neck cancer. Score 0-100, where a higher value means more symptoms.
Time Frame
1-4 years
Title
Alkaline phosphatase
Description
An increased value indicates an increase in bone metabolism
Time Frame
1-4 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 0-3. Ability to understand Swedish speech and writing. Received oral and written information about the study and given consent to participate in writing. Exclusion Criteria: 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 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Louise Sameby, MD
Phone
+46313436713
Email
louise.sameby@vgregion.se
First Name & Middle Initial & Last Name or Official Title & Degree
Göran Kjeller, Docent
Phone
+46104417750
Email
goran.kjeller@odontologi.gu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Göran Kjeller, Docent
Organizational Affiliation
Department of oral and maxillofacial surgery, Institute of odontology, Sahlgrenska Academy, GU
Official's Role
Study Director
Facility Information:
Facility Name
Department of oral and maxillofacial surgery, Institute of odontology, Sahlgrenska Academy, University of Gothenburg
City
Gothenburg
State/Province
Göteborg
ZIP/Postal Code
413 90
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Göran Kjeller, Docent
Phone
+46104417750
Email
goran.kjeller@odontologi.gu.se
First Name & Middle Initial & Last Name & Degree
Göran Kjeller, Docent
Facility Name
Department of Oral and Maxillofacial Surgery, The University Hospital of Skåne
City
Lund
State/Province
Skåne
ZIP/Postal Code
22242
Country
Sweden
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Martin N Bengtsson, DDS, PhD
Phone
+4646171769
Email
martin.n.bengtsson@skane.se
First Name & Middle Initial & Last Name & Degree
Martin N Bengtsson, DDS, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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The Effect of Hyperbaric Oxygen Treatment in Patients With Osteoradionecrosis.

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