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A prospective, multicenter, self-matched clinical trial for the evaluation of safety and efficacy of propofol in blood during general anesthesia by a medical blood concentration analyzer (ion migration spectrometry)

A prospective, multicenter, self-matched clinical trial for the evaluation of safety and efficacy of propofol in blood during general anesthesia by a medical blood concentration analyzer (ion migration spectrometry)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100872
Enrollment
Unknown
Registered
2025-04-16
Start date
2024-08-22
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

None

Interventions

Medical blood concentration analyzer (ion migration spectrometry) group:None

Sponsors

Shanghai Fourth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. 18-75 years old (including boundary value), gender unlimited. 2. Patients who are expected to undergo an operation and use propofol TCI anesthesia. 3. Clinical information are clear, complete and traceable, including subject's unique number (medical record number/clinic number /hospitalization number), gender, age, clinical symptoms/diagnostic information, etc. 4. American College of Anesthesiologists (ASA) grades I, II, III. 5. The subject or guardian can communicate well with the researcher, understand and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women. 2. Other subjects considered inappropriate to participate in this study, such as poor compliance.

Design outcomes

Primary

MeasureTime frame
Detection concentration ratio;

Secondary

MeasureTime frame
Detection accuracy;Detection time;Instrument performance evaluation;Usability evaluation;

Countries

China

Contacts

Public ContactChen guozhong

Shanghai Fourth People's Hospital

cgzssq2000@sina.com+86 139 6078 9827

Outcome results

None listed

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