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Study for comparing BIS index and BISpro index to monitor the accuracy of propofol sedation depth

Study for comparing BIS index and BISpro index to monitor the accuracy of propofol sedation depth

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024037
Enrollment
Unknown
Registered
2019-06-23
Start date
2019-08-01
Completion date
Unknown
Last updated
2019-10-14

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

Conditions

General anesthesia depth monitor

Interventions

Gold Standard:the BIS index for traditional anesthesia depth monitoring indicators
Index test:new BISpro index

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-64 year; 2. ASA I-II; 3. Elective patients undergoing hysteroscopic surgery.

Exclusion criteria

Exclusion criteria: 1. Long-term use of patients with sedative analgesics before surgery; 2, patients with cardiopulmonary dysfunction; 3. Patients with propofol or alcohol allergy; 4. Pregnant or lactating patients; 5, obese patients

Design outcomes

Primary

MeasureTime frame
BIS index;BISpro index;SEN, SPE, ACC, AUC of ROC;—

Countries

China

Contacts

Public ContactTao Luo

Peking University Shenzhen Hospital

luotao_wh@163.com+86 13510820779

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026