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Recruiting NCT06579040

NCT06579040 The HEROES Trial: Hyperbaric Oxygen Therapy for Endometriosis-Related Pain

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Clinical Trial Summary
NCT ID NCT06579040
Status Recruiting
Phase
Sponsor Sunnybrook Health Sciences Centre
Condition Endometriosis-related Pain
Study Type INTERVENTIONAL
Enrollment 64 participants
Start Date 2025-04-08
Primary Completion 2027-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Monoplace Hyperbaric Chamber (Class III medical device)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 64 participants in total. It began in 2025-04-08 with a primary completion date of 2027-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Endometriosis, is a condition where tissue from the uterus, called endometrium, grows outside of the uterus. This effects up to 10% of women, and can lead to long-lasting, moderate to severe pelvic pain, infertility and other symptoms. This can affect a woman's quality of life (including increased risk of depression and anxiety) and is associated with increased healthcare costs. Current treatments are often limited by serious side effects, and many women resort to surgery. Surgery is also associated with complications and there are long wait times for procedures, sometimes over 3 years. This means that many women continue to suffer from symptoms while they wait for surgery. Therefore, new effective treatments for endometriosis pain are needed. New research suggests that inflammation and stress caused by lack of oxygen in the affected areas may cause endometriosis. Hyperbaric Oxygen Therapy (HBOT), where patients are placed in a small chamber with higher than normal levels of oxygen, suppresses inflammation and promotes tissue healing. Because inflammation is central to this condition, HBOT has emerged as a potential treatment. In this study, the investigators will test if HBOT, in addition to the standard treatments, is more effective at treating endometriosis pain than the standard treatments alone.

Eligibility Criteria

Inclusion Criteria: * Age ≥ 18 years old * Patients having refractory pelvic pain (NRS≥4) secondary to endometriosis for \>6 months * May or may not be on traditional multi-modal treatment (pharmacological and/or non-pharmacological) * On waitlist for surgical treatment Exclusion Criteria: * Patients with chronic pain resulting from disease processes unrelated to the pathophysiology of endometriosis-related symptoms (e.g. irritable bowel syndrome, migraine headache, fibromyalgia, chronic low back pain, and musculoskeletal injuries) * Contraindications/medically unfit to receive hyperbaric treatments at an outpatient facility (e.g. pneumothorax, in-patients, requiring infusions to maintain hemodynamics, active and unstable coronary disease) * Unlikely to comply with follow-up assessments (e.g. no fixed address, plans to move out of town)

Contact & Investigator

Central Contact

Fahad Alam, MD

✉ fahad.alam@sunnybrook.ca

📞 416-480-4864

Frequently Asked Questions

Who can join the NCT06579040 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Endometriosis-related Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06579040 currently recruiting?

Yes, NCT06579040 is actively recruiting participants. Contact the research team at fahad.alam@sunnybrook.ca for enrollment information.

Where is the NCT06579040 trial being conducted?

This trial is being conducted at Toronto, Canada.

Who is sponsoring the NCT06579040 clinical trial?

NCT06579040 is sponsored by Sunnybrook Health Sciences Centre. The trial plans to enroll 64 participants.

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