MedPath

Hyperbaric Oxygen Therapy for Ulcerative Colitis Flares

Phase 2
Completed
Conditions
Colitis, Ulcerative
Interventions
Other: Hyperbaric Oxygen Therapy
Registration Number
NCT03494764
Lead Sponsor
Dartmouth-Hitchcock Medical Center
Brief Summary

Ulcerative colitis (UC) is a chronic inflammatory bowel disease associated with recurrent mucosal inflammation. Clinically, the disease is characterized by bloody diarrhea, abdominal pain, and constitutional symptoms such as fever and weight loss. Treatment strategies vary based on disease activity and target various aspects of the inflammatory cascade. Options include: anti-inflammatory drugs (mesalamine), immunosuppressive or modulatory medications (corticosteroids, thiopurines, cyclosporine) and biologic agents (Anti-TNF). Disease severity can be wide ranging, and nearly 25% of UC patients are hospitalized for acute severe disease. Of these patients, 30% will undergo colectomy after the acute episode, a quarter of which will experience post-operative complications. Although there has been great progress in treatment of UC over the past decade, even with the anti-TNF agent infliximab, the one-year remission rate for patients not responding to conservative management is barely 20%. Furthermore, corticosteroids have significant long-term consequences and immune suppressive drugs such as 6-mercaptopurine, azathioprine and infliximab have been associated with serious adverse events including life-threatening infections and lymphomas. With growing evidence that the pathogenesis of UC is multi-factorial and involves a complex interaction of genetic and environmental factors, newer treatment modalities are being evaluated to target the mucosal immune response and mucosal inflammatory regulatory system.

Hyperbaric oxygen offers a promising new treatment option since it targets both tissue hypoxia and inflammation. Recent small scales studies evaluating the impact of hyperbaric oxygen treatment in acute ulcerative colitis flares demonstrated improved outcomes. The mechanisms underlying the improvement are not known. In this study, we will treat ulcerative colitis flares with hyperbaric oxygen and measure changes in both markers of tissue hypoxia and inflammation. We hypothesize that hyperbaric oxygen will (a) improve outcomes, and (b) show reductions in markers of both tissue hypoxia and inflammation.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
39
Inclusion Criteria
  • Hospitalized patients with known or newly diagnosed moderate to severe ulcerative colitis (as defined by the Mayo score ≥6)

  • Consented within the first 48 hours of initiating IV steroids

  • Risk score of >3 points (pts)

    • Mean stool frequency/24 hrs (<4 = 0 pts, 4-6 = 1 pt, 7-9 = 2 pts, >9 = 4 pts)
    • Colonic Dilation = 4pts
    • Hypoalbuminemia (< 3mg/dL) = 1 pts
  • Mayo endoscopic sub-score >2 (moderate to severe)

  • Age >18 and able to make their own medical decisions

Exclusion Criteria
  • Complication requiring urgent surgical intervention (in the opinion of the investigators)

  • Clinically significant cardiac, renal, neurological, endocrine, respiratory or hepatic impairment in the opinion of the investigator, including but not limited to:

    • Pulmonary (COPD with CO2 retention; Previous/current imaging showing hyperinflation/air trapping/bullous disease/blebs (opinion of investigators), Current pneumothorax or previous spontaneous pneumothorax, Bronchogenic cyst(s))
    • Cardiac (Uncontrolled HTN (systolic >160 or diastolic >100), Unstable angina or myocardial infarction within the previous 3 months, Ejection fraction < 35%, Current or previous amiodarone use, ICD in place, Pacemaker in place not approved for chamber use)
    • Hematological/Oncological (Current chemotherapeutic drug use, and past history of bleomycin use,Hereditary Spherocytosis, Sickle cell anemia)
    • Gastrointestinal and Infectious Disease (Known or suspected Crohn's disease, Previous infection with mycobacterium, fungus, HIV, Hepatitis B or C, Severe gastrointestinal or systemic infection (opinion of investigator), Current capsule endoscopy or previously non-retrieved capsule
    • Endocrinology (Uncontrolled hyperthyroidism)
    • Neurological and Psychological (Vagal or other nerve stimulators, Uncontrolled seizure disorder, Medications or medical conditions that lower seizure threshold (opinion of the investigator), Drug or alcohol abuse/dependence,Current treatment for alcohol cessation with disulfiram, Current or recent (within past week) use of baclofen)
    • Head and Neck (Previous middle ear damage, surgery or infection(s) which may increase the risk for needing ear tubes (opinion of the investigator),Current or previous retinal detachment or optic neuritis, Retinal or vitreous surgery within the past 3 months)
  • Implanted devices not on the approved list for use with HBOT

  • Women who are pregnant or nursing. Women with childbearing potential were required to use effective birth control if not surgically sterile or postmenopausal for >2 years.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
3 Days Hyperbaric TherapyHyperbaric Oxygen TherapyPatients will be enrolled and follow an identical medical treatment algorithm. At day 3 responders (based on partial Mayo score) will be re-randomized in a 1:1 fashion to complete 5 total days of HBOT (1 session per day) or to stop after 3 days of HBOT. Non-responders will be entered into an open label arm to complete 5 total days of HBOT.
5 Days Hyperbaric TherapyHyperbaric Oxygen TherapyPatients will be enrolled and follow an identical medical treatment algorithm. At day 3 responders (based on partial Mayo score) will be re-randomized in a 1:1 fashion to complete 5 total days of HBOT (1 session per day) or to stop after 3 days of HBOT. Non-responders will be entered into an open label arm to complete 5 total days of HBOT.
Primary Outcome Measures
NameTimeMethod
Impact of HBOT on clinical response/remission5 Days

Impact of HBOT on clinical response/remission to medical therapy as measured by the partial Mayo score at study day 5.

Secondary Outcome Measures
NameTimeMethod
Flair durationday 5, 10

time to reduction in mayo score

microbiome compositionday 10

Describe the HBOT specific changes in the microbiome composition

relative and absolute reduction in the Mayo scoreDay 5, 10

Relative and absolute reduction in the Mayo score

Hospitalization durationday5, 10

time in the hospital

Relative and absolute change in inflammatory markersday 10

Relative absolute change in inflammatory markers: interleukins

proportion of patients requiring other therapyDay 5, 10

Proportion who require cyclosporine, infliximab or colectomy during index flare

Relative and absolute change in gene expressionday 10

Relative absolute change in gene expression: HO-1

Trial Locations

Locations (8)

UC San Diego Health Systems

🇺🇸

La Jolla, California, United States

University of Maryland

🇺🇸

Baltimore, Maryland, United States

University of California San Diego

🇺🇸

San Diego, California, United States

Dartmouth-Hitchcock Medical Center

🇺🇸

Lebanon, New Hampshire, United States

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

NYU Langone Medical Center

🇺🇸

New York, New York, United States

University of Texas Southwestern Medical Center

🇺🇸

Dallas, Texas, United States

Virginia Mason Memorial Hospital

🇺🇸

Yakima, Washington, United States

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