Skip to content

Protective Effects of Dexmedetomidine on Myocardial Injury During Liver Transplantation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03013634
Enrollment
100
Registered
2017-01-06
Start date
2016-10-31
Completion date
2017-11-30
Last updated
2017-01-06

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

Conditions

Evidence of Liver Transplantation, Myocardial Injury

Keywords

dexmedetomidine

Brief summary

The purpose of this study was to evaluate the protective effect of dexmedetomidine on myocardial injury during liver transplantation

Detailed description

Liver transplantation surgery may lead to myocardial injury. Dexmedetomidine, a highly specific α2-adrenoeptor agonist, has sedative and analgesic properties without significant respiratory depression at the clinically approved dosage. Some investigations indicated that dexmedetomidine was able to protect the myocardium via improving the activity of Na+-K+-adenosine triphosphate enzyme and Ca2+-adenosine triphosphate, alleviating inflammation reaction and avoiding Ca2+ overload. However, the effect and the mechanism of dexmedetomidine on myocardial injury during liver transplantation remain unclear.

Interventions

DRUGDexmedetomidine

Dexmedetomidine infusion:loading 0.5ug/kg for 10min, then 0.5 ug/kg/h until the end of operation.

DRUGNormal saline

Equal volume normal saline substitute for dexmedetomidine

Sponsors

Tianjin First Central Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* End stage liver disease scheduled for liver transplantation in Tianjin First Center Hospital

Exclusion criteria

* Pre-existing respiratory failure,renal failure,hepatic encephalopathy

Design outcomes

Primary

MeasureTime frame
Peri-operative mortalitythrough study completion, an average of 5 weeks
The incidence of cardiac complicationsfrom anesthesia induction to 24 hours after operation

Secondary

MeasureTime frameDescription
Evidences of Clinically Definite Myocardial Injury Confirmed by Electrochemiluminescencebefore skin incision, 0.5 hour min after anhepatic, 2 hours of neohepatic stage,the end of surgery,24 hours after operationmyohemoglobin,creatine kinase isoenzyme,cardiac troponinⅠ,Heart-type fatty acid-binding protein

Other

MeasureTime frameDescription
Length of ICU staythrough study completion, an average of 5 days
length of staythrough study completion, an average of 6 weeksfrom date of admission to discharge time

Countries

China

Contacts

Primary ContactWenli Yu, PhD
yzxyuwenli@163.com86-13920098326

Outcome results

None listed

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