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Brain Protection Effect of Selective Head Cooling and Dexmedetomidine in Patients Undergoing Liver Transplantation

Cerebral Protection Effect of Selective Head Cooling and Dexmedetomidine in Patients Undergoing Liver Transplantation

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03102359
Enrollment
100
Registered
2017-04-05
Start date
2017-04-05
Completion date
2019-12-31
Last updated
2019-05-29

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

Conditions

Liver Transplant; Complications

Brief summary

The investigators investigated in the present study whether selective head cooling and dexmedetomidine has an effect on cerebral oxygenation during liver transplantation and has cerebral protective effect in patients undergoing liver transplantation.

Interventions

DRUGDexmedetomidine

Using dexmedetomidine at anesthesia induction and maintain until the end of the surgery

Using cooling helmet for selective head cooling group and Selective Head Cooling and Dexmedetomidine group

Sponsors

Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Scheduled for OLT, selected from the Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, China. * Sign the informed consent

Exclusion criteria

* The patients with a history of neurological or psychiatric disorders which impair cognitive processes, including previously established de-mentia, stroke, schizophrenia and depression were excluded from the study. * Patients diagnosed with hepatic encephalopathy or had a low Mini-Mental State Examination (MMSE) score (below 24) preoperatively. * With concurrent diseases such as renal insufficiency, diabetes mellitus were also excluded. * Patients were excluded if severe reperfusion syn-drome (mean arterial pressure below 60mmHg sustained over 15minutes) occurred perioperatively.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative minimal hepatic encephalopathy (MHE)14 days after surgeryUsing PSE-Syndrom-Test

Countries

China

Contacts

Primary ContactAilin Luo, doctorate
alluo@tjh.tjmu.edu.cn13507122565

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026