Skip to content

Validation of the accuracy of brain tissue oxygen saturation monitor

Validation of the accuracy of brain tissue oxygen saturation monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052321
Enrollment
Unknown
Registered
2021-10-24
Start date
2019-06-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

none

Interventions

experimental group:Stepped Hypoxia

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1. Healthy adults aged 18 ~ 45 years old, with balanced and reasonable gender distribution; 2. Subject: carbon monoxide hemoglobin COHb 10g / dl; 5. No smoking history / no smoking history; 6. No previous history of cardiopulmonary disease; 7. Those who pass the physical examination; 8. Subjects voluntarily participate in clinical trials and voluntarily sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. Smokers or those exposed to high carbon monoxide content; 2. Those with coagulation dysfunction or artificial blood vessels; 3. Those with previous cardiopulmonary diseases; 4. There is skin disease, infection or trauma around the measurement site, which makes the parameter unable to be measured; 5. Patients with mental illness, epilepsy or other diseases leading to involuntary movement of the body; 6. Physical condition will lead to the increase of methemoglobin; 7. If the operation carried out during the clinical trial may cause excessive medical risk to the subjects, such subjects shall be excluded; 8. Pregnant women; 9. Those with grey nails; 10. The clinical trial personnel judge that the compliance is not good and cannot strictly implement the scheme; 11. Subjects are enrolled in other clinical trials within 30 days; 12. There are other diseases that are not suitable for clinical trial; 13. Unwilling to sign informed consent.

Design outcomes

Primary

MeasureTime frame
regional cerebral tissue oxygen saturation (rSO2 );

Countries

China

Contacts

Public ContactZongze Zhang

Zhongnan Hospital of Wuhan University

zhangzz_0301@126.com+86 13971687403

Outcome results

None listed

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