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The effect of S-ketamine on postoperative neurocognitive function in patients undergoing heart valve replacement surgery

The effect of S-ketamine on postoperative neurocognitive function in patients undergoing heart valve replacement surgeryQYFY

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082881
Enrollment
Unknown
Registered
2024-04-10
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Delayed neurocognitive recovery(dNCR)

Interventions

S-ketamine group:During anesthesia induction, a single intravenous injection of 0.3-0.5mg/kg S-ketamine is administered, followed by continuous intravenous infusion of 0.3mg/kg/h S-ketamine during sur
control group:Inject equal volume of physiological saline during anesthesia induction, and administer continuous intravenous infusion of equal volume of physiological saline during surgery

Sponsors

Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age = 18 years old; 2. The American Society of Anesthesiologists (ASA) grades I-IV; 3. Accept heart valve replacement surgery; 4. Voluntarily participate in the experiment and sign an informed consent form

Exclusion criteria

Exclusion criteria: 1. Previous presence of dementia, Parkinson's disease, epilepsy, or mental illness; 2. Preoperative Mini Mental State Scale (MMSE) score<18, indicating neurocognitive impairment; 3. Previous history of cerebral infarction, cerebral hemorrhage, and traumatic brain injury, with a history of being thick and robust as a sequelae; 4. Regular use of sedatives or antidepressants may lead to alcohol or illegal drug abuse disorders. 5. Existence of visual and auditory barriers, or inability to speak Mandarin and communicate; 6. Allergy to S-ketamine 7. Patients with concomitant aortic dissection, pheochromocytoma, intracranial aneurysm, and other diseases 8. Patients with coexisting sinus bradycardia (heart rate<50 beats/min), pathological sinus syndrome, or second degree atrioventricular block or above, or severe cardiac dysfunction that prevents assessment from being completed 9. Patients with severe liver dysfunction (child pugh grade C) and/or renal dysfunction (currently undergoing dialysis treatment)

Design outcomes

Primary

MeasureTime frame
The incidence rate of dNCR;

Secondary

MeasureTime frame
white blood cell,WBC;C-reactive protein,CRP;neutrophil-to-lymphocyte ratio,NLR;Procalcitonin,PCT;IL-6 IL-1ß;

Countries

China

Contacts

Public ContactZejun Niu

Affiliated Hospital of Qingdao University

nzj16niu@sina.com+86 186 6180 5522

Outcome results

None listed

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