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A prospective nested case-control study on immediate postoperative hypozincemia and the risk of delirium in elderly non-cardiac surgery patients

A prospective nested case-control study on immediate postoperative hypozincemia and the risk of delirium in elderly non-cardiac surgery patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120093
Enrollment
Unknown
Registered
2026-03-09
Start date
2026-03-09
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Postoperative delirium

Interventions

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 65 to 90 years; 2. Patients scheduled for elective urological, orthopedic, general surgical, or thoracic surgical procedures; 3. Moderate-to-major surgeries with an anticipated duration >=1 hour; 4. Expected postoperative hospital stay >=72 hours; 5. American Society of Anesthesiologists (ASA) Physical Status Classification of II–III; 6. Patients with normal preoperative cognitive function (Montreal Cognitive Assessment, Version 8.1 score >=22); 7. Patients or their legally authorized representatives provided informed consent and agreed to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with a documented history of psychiatric or neurological disorders, such as depression, severe central nervous system depression, schizophrenia, epilepsy, Parkinson's disease, or Alzheimer's disease; 2. Individuals unable to undergo cognitive testing due to hearing or visual impairments; 3. Preoperative use of psychotropic medications or opioids; 4. Presence of preoperative conditions affecting normal communication, including delirium, coma, or dementia; 5. Patients with severe cardiac disease (NYHA Class III or IV), hepatic insufficiency (Child-Pugh Class C), severe renal dysfunction (estimated glomerular filtration rate 3 months) use of zinc supplements prior to surgery; 8. Current participation in other clinical trials; 9. Planned secondary surgical procedures within 7 days postoperatively.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative delirium;

Secondary

MeasureTime frame
Duration of delirium;Severity of postoperative delirium;Perioperative electroencephalography and related EEG parameters;Postoperative recovery quality QoR15;Resting and exercise NRS score;Incidence of postoperative nausea and vomiting (PONV);30-day all-cause mortality rate;Incidence of complications after surgery;

Countries

China

Contacts

Public ContactChen Lijian

The First Affiliated Hospital of Anhui Medical University

chenlijian77@126.com+86 139 6669 9467

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026