Skip to content

Efficacy and Influencing Factors of Hyperbaric Oxygen Therapy in Patients with Moderate to Severe Traumatic Brain Injury: A Multicenter, Prospective, Observational Study(ECHO-TBI)

Efficacy and Influencing Factors of Hyperbaric Oxygen Therapy in Patients with Moderate to Severe Traumatic Brain Injury: A Multicenter, Prospective, Observational Study - ECHO-TBI

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106244
Enrollment
Unknown
Registered
2025-07-21
Start date
2025-07-21
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Moderate to Severe Traumatic Brain Injury

Interventions

The conventional hyperbaric oxygen therapy group:None
The unconventional hyperbaric oxygen therapy group:None

Sponsors

Beijing Chaoyang Hospital , Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1)Based on the medical history, and confirmed by cranial CT scans and clinical symptoms, the diagnosis is traumatic brain injury with a Glasgow Coma Scale (GCS) score of less than 13 points; 2)Aged between 18 and 75 years; 3)The interval from onset of illness to the first session of hyperbaric oxygen therapy is <=3 months; 4)The patient or their family members (for patients with impaired consciousness or cognitive impairment) are aware of this study and voluntarily participate, and all have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1)A history of severe cerebral hemorrhage or cerebral infarction within the past 3 months; 2)Severe dysfunction of vital organs such as the heart, liver, lungs, or kidneys; 3)Malignant tumors, hematologic diseases, or coagulation disorders; 4)A history of mental illness or a family history of mental illness; 5)Pregnant or breastfeeding women; 6)Incomplete clinical data; 7)Currently participating in research studies involving other drugs or medical devices; 8)Spinal cord injury; 9)Recovery of the Glasgow Coma Scale (GCS) score to greater than 13 points within 48 hours after injury.

Design outcomes

Primary

MeasureTime frame
The DRS scores ;

Secondary

MeasureTime frame
The mRS scores ;Barthel index;all-cause mortality;Incidence of adverse reactions;

Countries

China

Contacts

Public ContactJing Yang

Beijing Chaoyang Hospital, Capital Medical University

CYHospitalCYHBO@yeah.net+86 138 1157 2858

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026