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Clinical Trial Protocol for Evaluating CRT Pulse Oximetry Accuracy

Clinical Trial Protocol for Evaluating CRT Pulse Oximetry Accuracy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124176
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-05-08
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

None

Interventions

Controlled Desaturation Study:Controlled Desaturation

Sponsors

Shenzhen Nanshan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Healthy adults, male and female, aged 18-45 years, must understand the clinical trial and voluntarily participate in and sign informed consent; (2) Meet the American Society of Anesthesiologists (ASA) grade I; (3) Subjects' hemoglobin COHb10g/dL; (4) Allen's test was negative (indicating that the ulnar artery had good blood supply and the radial artery could be used for puncture);

Exclusion criteria

Exclusion criteria: (1) the subject had any systemic disease or methemoglobinemia; (2) smokers or those exposed to high levels of carbon monoxide; (3) pregnancy; (4) the subjects had symptoms or history of peripheral ischemia;

Design outcomes

Primary

MeasureTime frame
Pulse oxygen saturation;

Countries

China

Contacts

Public ContactFeng Guangju

Shenzhen Nanshan People's Hospital

fenggjsz@163.com+86 13823635608

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026