Hyperbaric Oxygen Therapy for Radiation Injury

Soft Tissue Radiation Injury; Patient Reported Evaluation in a Single Centre Cohort Study (STRIPE)

Recruiting Observational Study
Cystitis, Radio Induced Soft Tissue Radionecrosis (STRN) Radiation Proctitis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
Karolinska University Hospital · Other
Who this trial is looking for

This trial is looking for adults with late radiation tissue injury who have received hyperbaric oxygen therapy (HBOT). Participants will help researchers understand how effective this treatment is and who benefits the most from it.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am an adult over 18 years old
  • I have late radiation tissue injury
  • I have been treated with hyperbaric oxygen therapy

You may not be able to join if

  • I have requested not to be included in the study
  • I have not signed informed consent

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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About This Trial
Radiotherapy cures many cancers but can cause late radiation-induced tissue injury (LRTI), leading to long-term symptoms from the bladder and bowel and reduced health-related quality of life (HRQoL). Hyperbaric oxygen therapy (HBOT) is an established treatment that reduces chronic inflammation and promotes tissue repair. Randomized studies have demonstrated improvements in symptoms and quality of …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult patients (\>18 years old) * Late radiation tissue injury * Treated with HBOT Exclusion Criteria: * Requested not to be included in the study (Retrospective cohort) * Not signed informed consent (Prospective cohort)
Contacts

Anders Kjellberg, MD, PhD

+46760657355

anders.kjellberg@regionstockholm.se

CONTACT