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To study the relationship between nociceptive stimulation index (qnox) and delirium after knee arthroplasty in the elderly

To study the relationship between nociceptive stimulation index (qnox) and delirium after knee arthroplasty in the elderly

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059985
Enrollment
Unknown
Registered
2022-05-14
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

knee arthroplasty

Interventions

two:Qnox monitoring
one:BIS monitoring

Sponsors

anhui provincial hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients who plan to undergo knee replacement (including total knee replacement and single condylar replacement); 2. American Association of Anesthesiologists (ASA) grading II - III; 3. Age = 65 years; 4. Preoperative MMSE score = 17 points.

Exclusion criteria

Exclusion criteria: 1. Patients with cognitive impairment, mental illness or dementia before operation; 2. Patients with severe organic diseases (coronary heart disease, bronchial asthma, severe hypertension, severe blood system dysfunction, liver and kidney function, and electrolyte abnormalities); 3. Have a long history of abuse of sedatives or analgesics; 4. Those who have participated in clinical trials of other drugs in the past 4 weeks.

Design outcomes

Secondary

MeasureTime frame
C-reactive protein;Postoperative Recovery Quality Scale-15;

Primary

MeasureTime frame
postoperative delirium;Postoperative pain score;

Countries

China

Contacts

Public ContactWang sheng

Anhui provincial hospital

iamsheng2020@ustc.edu.cn+86 19156007726

Outcome results

None listed

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