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Cerebral protection by dexmedetomidine-ketamine and dexmedetomidine-remifentanil after cardiac replacement with cardiopulmonary bypass:a comparative study

Cerebral protection by dexmedetomidine-ketamine and dexmedetomidine-remifentanil after cardiac replacement with cardiopulmonary bypass:a comparative study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018767
Enrollment
Unknown
Registered
2018-10-09
Start date
2018-10-08
Completion date
Unknown
Last updated
2018-10-15

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

Conditions

Brain damage

Interventions

Group 2:In the DK group, dexmedetomidine (0.2-0.7) was administered with g/kg/h and ketamine (0.3-0.5) mg/kg/h intravenous pump
Group 1:The use of dexmedetomidine same as DF group, with efflux g/kg/h after fentanyl (0.5~1.0).

Sponsors

Department of Intensive Medcine, Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. undergoing elective patients with heart valve replacement operation under CPB, ASA class I-III; Heart function class I-III; 2. Body mass index of 18.5 ~ 23.9 kg / ?;Subjects were assessed on the preoperative simple mental status examination scale at 27 points on > and expected CPB time at > for 30 minutes.

Exclusion criteria

Exclusion criteria: 1. With important organ diseases such as liver and kidney, history of cerebrovascular and neuropsychiatric diseases, and brain trauma surgery; 2. with history of cerebrovascular accident in patients with severe hypertension, hypotension or bradycardia; Those with increased intracranial pressure, such as intracranial aneurysm and intracranial tumor, etc.; 3. With increased intraocular pressure; 4. Patients with hyperthyroidism and adrenal pheochromocytoma; 5. Patients with epilepsy and schizophrenia; 6. Patients with sinus bradycardia or hypotension; 7. Patients with difficulty in communication (such as hearing or speech communication); 8. The patient who refused to participate in this trial.

Design outcomes

Primary

MeasureTime frame
S-100ß protein, neuron specific enolase;

Countries

China

Contacts

Public ContactZhao Wenjing

Department of Intensive Medcine, Affiliated Hospital of Xuzhou Medical University

zhaowj@886.com+86 13852157285

Outcome results

None listed

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