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Hyperbaric Oxygen Therapy for Sarcoma
Phase 4
Recruiting
Led By William Eward, MD, DVM
Research Sponsored by Duke University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Diagnosis of soft tissue sarcoma confirmed by an approved reference pathologist
Sarcoma of lower extremity location
Must not have
Active treatment with chemotherapy
Actively uncontrolled diabetes mellitus (A1c>8)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 weeks postoperatively
Awards & highlights
No Placebo-Only Group
Pivotal Trial
Drug Has Already Been Approved
Summary
This trial is testing if breathing pure oxygen in a pressurized room can help patients with leg sarcoma heal better after surgery and radiation. The extra oxygen might speed up their recovery. Hyperbaric oxygen therapy (HBOT) has been shown to have beneficial effects in the treatment of late radiation sequelae.
Who is the study for?
Adults aged 18-85 with soft tissue sarcoma in the lower extremity, who will have surgery after neo-adjuvant radiation therapy. Participants must not have had prior radiation in the area, be on high dose steroids or chemotherapy, have uncontrolled diabetes, active deep vein thrombosis, or compromised blood flow to the limb.
What is being tested?
The study is testing if hyperbaric oxygen therapy (HBOT) improves wound healing post-surgery for soft tissue sarcoma patients compared to standard care. Patients are randomly placed into two groups: more will receive HBOT and fewer will get standard care.
What are the potential side effects?
Possible side effects of HBOT include ear pain due to pressure changes, temporary vision changes, fatigue, and rarely lung collapse or seizures from too much oxygen.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My soft tissue sarcoma diagnosis has been confirmed by a specialist.
Select...
My sarcoma is located in my leg.
Select...
I am scheduled for radiation therapy before surgery to remove my tumor.
Select...
My surgery wound is expected to be closed primarily.
Select...
My blood flow in limbs hasn't been reduced by surgery.
Select...
I haven't had radiation or surgery on the tumor area before now.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently receiving chemotherapy.
Select...
My diabetes is not well-controlled (A1c>8).
Select...
I have an active blood clot in the limb being treated.
Select...
I have had radiation or surgery on the tumor area before this treatment.
Select...
I am taking more than 5mg of prednisone or its equivalent daily.
Select...
I have had surgery on a limb that affected its blood flow.
Select...
My blood flow to the limb getting treatment is poor due to vascular disease.
Select...
I am younger than 18 or older than 85.
Select...
My treatment plan does not include pre-surgery radiation or surgery to remove the tumor.
Select...
My sarcoma is not located in my lower extremity.
Select...
I am scheduled for radiation therapy after surgery.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 weeks postoperatively
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 weeks postoperatively
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Hyperbaric Treatment Completion Rate
Participant Assessment Form Completion Rate
Recruitment rate
+3 moreSecondary study objectives
Frequency of delayed wound healing
Frequency of surgical site infections or periprosthetic infections
Variability in Patient Reported Quality of Life
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Hyperbaric Oxygen GroupExperimental Treatment1 Intervention
Patients will receive Hyperbaric Oxygen treatments in the immediate postoperative period
Group II: Standard of Care GroupActive Control1 Intervention
Patients will not receive Hyperbaric Oxygen treatments in the immediate postoperative period
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Hyperbaric oxygen
2013
Completed Phase 4
~360
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for sarcoma include chemotherapy, radiation therapy, and hyperbaric oxygen therapy (HBOT). Chemotherapy targets and kills rapidly dividing cancer cells, which helps in shrinking tumors.
Radiation therapy damages the DNA of cancer cells, leading to their death and reducing tumor size. HBOT increases oxygen availability in tissues, enhancing the effectiveness of radiation therapy and promoting better wound healing post-surgery.
These mechanisms are vital for sarcoma patients as they improve surgical outcomes, reduce tumor burden, and potentially increase survival rates.
[Co-operation of fundamental research with clinical work in radiation oncology].Tumour oxygenation under normobaric and hyperbaric conditions.
[Co-operation of fundamental research with clinical work in radiation oncology].Tumour oxygenation under normobaric and hyperbaric conditions.
Find a Location
Who is running the clinical trial?
Duke UniversityLead Sponsor
2,452 Previous Clinical Trials
2,971,771 Total Patients Enrolled
William Eward, MD, DVMPrincipal InvestigatorDuke Health
2 Previous Clinical Trials
65 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am between 18 and 85 years old.My treatment plan includes radiation before surgery.My surgery wound is expected to be closed primarily.My surgery wound is expected to be closed primarily.My cancer can be of any stage, grade, or type.My blood flow in limbs hasn't been reduced by surgery.I have had radiation or surgery on the tumor area before this treatment.I am taking more than 5mg of prednisone or its equivalent daily.I have had surgery on a limb that affected its blood flow.My blood flow to the limb getting treatment is poor due to vascular disease.I haven't had radiation or surgery on the tumor area before now.I am younger than 18 or older than 85.My treatment plan does not include pre-surgery radiation or surgery to remove the tumor.My sarcoma is not located in my lower extremity.I am scheduled for radiation therapy after surgery.My diabetes is not well-controlled (A1c>8).My cancer can be of any severity.I am currently receiving chemotherapy.I have an active blood clot in the limb being treated.My soft tissue sarcoma diagnosis has been confirmed by a specialist.My sarcoma is located in my leg.I am scheduled for radiation therapy before surgery to remove my tumor.My blood flow in my limbs is normal and hasn't been affected by surgery.My soft tissue sarcoma diagnosis has been confirmed by a specialist.My cancer can be of any tissue type.My condition is at any stage of disease.
Research Study Groups:
This trial has the following groups:- Group 1: Hyperbaric Oxygen Group
- Group 2: Standard of Care Group
Awards:
This trial has 3 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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