Adjunct Targeted Temperature Management in Acute Severe Carbon Monoxide Poisoning
Launched by WONJU SEVERANCE CHRISTIAN HOSPITAL · Jul 13, 2021
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at how different temperature management strategies can affect the recovery of patients who have suffered from severe carbon monoxide poisoning, a serious condition that can affect brain function. The study will compare two methods: one group of patients will receive a treatment called therapeutic hypothermia, which involves cooling the body to a lower temperature, while the other group will be kept at normal body temperature. Both groups will also receive hyperbaric oxygen therapy, which is a special treatment using pure oxygen to help the body heal.
To participate in this trial, individuals must be at least 19 years old and have received hyperbaric oxygen therapy within 24 hours of their carbon monoxide poisoning. They should also show signs of severe poisoning, such as being unable to respond verbally after treatment. However, those who have had a cardiac arrest before receiving the therapy, have serious pre-existing health issues, or are pregnant cannot join. Participants will be closely monitored throughout the study and will help researchers understand how to improve care for future patients with this dangerous condition.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • ≥ 19 years.
- • Patients who received HBO within 24 hours for acute CO poisoning.
- • Patients who meet the definition of ASCOP (Patients incapable verbal obey after HBO).
- • Signed informed consent prior to study entry.
- Exclusion Criteria:
- • Cardiac arrest before HBO
- • Previous neurocognitive disorders
- • Life-threatening underlying disease (ex: advanced cancer)
- • Evidence of co-ingestion of sedative or hypnotics confirmed by intravenous flumazenil administration or history taking at the emergency department
- • Absolute contraindication for TH (active severe bleeding and profound shock not controlled by vasoactive drugs)
- • No admission
- • The significant co-ingested drug levels, which are alter the consciousness, is confirmed from the drug analysis lab
- • Pregnancy
- • Burns
- • More than moderate burn or Inhalation burn
- • Burns complicated by other trauma
- • Electrical burn
- • Burns in high risk patients (Patients with chronic underlying diseases (i.e DM, ESRD, liver cirrhosis, etc) which may cause delays or aggravate the wound healing)
About Wonju Severance Christian Hospital
Wonju Severance Christian Hospital is a leading healthcare institution based in South Korea, renowned for its commitment to innovative medical research and high-quality patient care. As a prominent clinical trial sponsor, the hospital is dedicated to advancing medical knowledge through rigorous scientific studies and trials across various therapeutic areas. With a multidisciplinary team of experienced researchers and healthcare professionals, Wonju Severance Christian Hospital strives to improve treatment outcomes and enhance the overall health and well-being of patients. Its state-of-the-art facilities and adherence to ethical standards ensure a robust framework for conducting clinical research that meets both local and international regulatory requirements.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Incheon, , Korea, Republic Of
Wonju, Gangwon, Korea, Republic Of
Patients applied
Trial Officials
Yong Sung Cha, MD
Principal Investigator
Wonju Severance Christian Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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