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NCT Number: NCT06579040

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Sunnybrook Health Sciences Centre

Toronto, Ontario, M4N 3M5, Canada

Location status: Recruiting

Location contact

Catherine Parry

CONTACT

About this study

Endometriosis is caused when endometrial-like tissue is found outside of the uterus. It predominantly affects women of reproductive age, with an estimated prevalence of 10% worldwide. Chronic pain related to endometriosis is one of the primary manifestations that lead individuals to seek treatment, with many women reporting moderate to severe pain that can have serious consequences for mental health and quality of life.

Current therapeutic approaches for endometriosis include hormonal therapies (e.g. oral contraceptive pills, progestins, and Gonadotropin-Releasing Hormone agonists/antagonists). While these treatments may provide temporary symptom relief, they are often associated with serious side effects and preclude conception during treatment. The efficacy of other medical interventions remains controversial, therefore surgical procedures are often indicated. However, surgery also has associated risks, has long wait times (between 6 months and 3 years), and a considerable percentage of patients experience recurrence of pain following surgical resection.

Pathologically, endometriosis is characterized by angiogenesis, inflammation, and a chronic hypoxic state at the cellular level. Because of this, Hyperbaric Oxygen Therapy (HBOT), which suppresses inflammation and promotes tissue healing, offers promise as a novel therapeutic modality. This is supported by murine models, which demonstrate the ability of HBOT to reduce inflammation and inflammatory cytokines in the context of endometriosis in animals. However, there have not been any human studies investigating the use of HBOT for treatment of endometriosis and related pain.

This study aims to explore HBOT as a treatment for endometriosis related pelvic pain. Specifically, the investigators will test if HBOT, in addition to the standard treatments (e.g. hormonal and non-hormonal medical options), is more effective at treating endometriosis pain than the standard treatments alone.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Monoplace Hyperbaric Chamber (Class III medical device)

Device

Participants in the intervention group will be triaged to the closest hyperbaric facility to their address and treated with 40 HBOTs (2 ATM for 90 mins, scheduled daily from Monday to Friday). As HBOT is not a service currently offered at Sunnybrook Hospital, all HBOT treatments will be provided at three collaborating outpatient facilities, Halton Hyperbaric Unit, Restore Hyperbaric Oxygen & Medical Centre (CPSO-certified Level-II OHP), and Rouge Valley Hyperbaric Medical Centre. All three facilities have the exact same hyperbaric chambers, run by anesthesiologists with advanced training, thus treatments will be identical at all sites.

Primary outcomes

  1. Change in pain symptoms on the NRS

    Time frame: At baseline, weekly for the first 8 weeks after enrollment, then at 3/4/5/6 month follow ups

    Assessed on the numeric rating scale between 0 to 10, with 10 indicating the worst possible pain

Secondary outcomes

  1. Change in pain frequency

    Time frame: At baseline, weekly for the first 8 weeks after enrollment, then at 3/4/5/6 month follow ups

    The change in pain frequency will be assessed on a 5-point Likert scale, where 1 is "never" and 5 is "always."

  2. Change in opioid consumption

    Time frame: At baseline, weekly for the first 8 weeks after enrollment, then at 3/4/5/6 months

    Collected as a categorical variable ("Are you taking 1) more, 2) same or 3) less compared to start of treatment?")

  3. Participant Quality of Life on the EHP-30

    Time frame: At baseline, and every month for 6 months

    The Endometriosis Health Profile-30 is a validated, high-sensitivity, 30-item endometriosis-specific assessment tool for capturing the impact of endometriosis on patient's lives.

  4. Participant Quality of Life on the SF-36

    Time frame: At baseline, and every month for 6 months

    The Quality of Life Short Form Survey-36 is a widely used tool to assess an individual's overall health-related quality of life.

Other outcomes

  1. Adherence to HBOT protocol

    Time frame: At 8 weeks (or last session)

    How many patients complete protocol (minimum 4 treatments per week with >35 treatments)

  2. Satisfaction assessed by a Patient Satisfaction Questionnaire

    Time frame: At 8 weeks (or last session) and 6 months following enrollment

    Subjective questionnaire completion at end of treatment inquiring about HBOT experience, barriers to and promoters of treatment

  3. Cost of study completion

    Time frame: Throughout study completion, an average of 6 months

    Cost of study completion on a per patient basis including research support, healthcare resource costs, and patient-related personal costs (transport, time from work)

Study contacts

Contact information is provided by the study sponsor or research team.

Fahad Alam, MD

CONTACT

[email protected]

416-480-4864

Grace Liu, MD

CONTACT

[email protected]

416-480-6100 ext. 65063

Sponsors and collaborators

Lead sponsor

Sunnybrook Health Sciences Centre

Other

Registry information

Official study title

The HEROES Trial: Hyperbaric Oxygen Therapy for Endometriosis-Related Pain: A Prospective Randomized Study

Acronym: HEROES

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Aug 30, 2024
Registry last updated
Apr 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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