This is an observational patient registry of COVID-19 patients treated with HBOT.
The retrospective analysis will focus on the reduction in need for mechanical ventilation in
COVID-19 patients. The information will be gathered prospectively. Data will be collected
from the patients' medical record, including medical notes and data recorded into the study
database.
Inclusion Criteria:
- Adult patients with COVID-19.
- The clinical decision to use HBOT is independent of the decision to participate in
registry.
- A signed and dated informed consent form for the off-label use of Hyperbaric Oxygen
Therapy specific to the institution where treatment is rendered.
- Subject is willing and able to comply with instructions and scheduled visits.
Exclusion Criteria:
- The Subject has other concurrent conditions that in the opinion of the Investigator
may compromise patient safety.
- The patient has an untreated pneumothorax.
White River Wound Healing Center
Batesville, Arkansas, United States
Community Hospital
Monterey, California, United States
Innovative Healing Systems
Tampa, Florida, United States
Decatur Memorial Hospital
Decatur, Indiana, United States
Providence Medical Wound Care Center
Kansas City, Kansas, United States
West Jefferson Medical Center
Marrero, Louisiana, United States
The Wound Treatment Center
Opelousas, Louisiana, United States
Christus Shreveport Bossier Hyperbaric & Wound Care Center
Shreveport, Louisiana, United States
Ascension Providence Rochester Hospital Wound Care Center
Rochester, Michigan, United States
CHI
Chattanooga, Tennessee, United States
Klinika Baromedical
Poznan, Wielkopolskie, Poland
Thomas E Serena, MD, Study Director
SerenaGroup, Inc.