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Monitoring nociceptive state with nociception index during general anesthesia: a prospective randomized controlled trial

Monitoring nociceptive state with nociception index during propofol–remifentanil anesthesia: a prospective randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045239
Enrollment
Unknown
Registered
2021-04-09
Start date
2021-04-08
Completion date
Unknown
Last updated
2021-11-16

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

Conditions

Complication after general anesthesia

Interventions

NOX group:Measuring with NOX

Sponsors

Third Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Patients undergoing elective non-heart and organ transplant surgery under general anesthesia for tracheal intubation; 3. It is ethical, the patient takes the test voluntarily and signs the informed consent form; 4. Operation time >= 1 hour.

Exclusion criteria

Exclusion criteria: 1. People suffering from mental or nervous system diseases or suspected dementia or memory impairment; 2. People with severe impairment of auditory, visual, and language system functions; 3. People who have cognitive dysfunction determined by the MMSE scale before surgery; 4. Determined/suspected to have abused or long-term use of narcotic sedatives and analgesics.

Design outcomes

Primary

MeasureTime frame
Number of episodes of inadequate anesthesia;

Secondary

MeasureTime frame
Anesthetics Consumption;Recovery Times;VAS score;

Countries

China

Contacts

Public ContactHei Ziqing

The Third Affiliated Hospital, Sun Yat-Sen University

heiziqing@sina.com+86 18922102601

Outcome results

None listed

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