Dexmedetomidine, Liver Transplantation, Allograft Function, Survival Clinical Trial
Official title:
Evaluation of the Impact of Dexmedetomidine on Allograft Function Recovery and Survival Following Liver Transplantation: A Randomised Control Trial
| Verified date | August 2023 |
| Source | RenJi Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
1.1. Background 1.1.1. Perioperative ischaemia/reperfusion (I/R) injury during liver transplantation is strongly associated with early allograft dysfunction, graft loss, and mortality. 1.1.2. Hepatic I/R injury also causes remote damage to other organs including the renal and pulmonary systems. 1.1.3. Dexmedetomidine, a selective α2-adrenoceptor agonist which is widely used as an adjuvant to general anaesthesia, has been widely shown in preclinical studies to provide organoprotection by ameliorating the effects of I/R injury in a range of tissues (including the liver). However, prospective clinical evidence of any potential benefits in improving outcomes in liver transplantation is lacking. 1.2. Objectives 1.2.1. To investigate the hypothesis that perioperative treatment with dexmedetomidine reduces the incidence of early allograft dysfunction and primary graft non-function in deceased donor liver transplantation. 1.2.2. The impact of dexmedetomidine on postoperative renal and pulmonary function will also be examined. 1.3. Study Design This is a prospective, single-centre, randomised, parallel-group study. 1.4. Setting Departments of Anesthesiology, Renji Hosptial, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China. 1.5. Patients 200 patients (18-65 years) scheduled to undergo liver transplantation under general anaesthesia. 1.6 Intervention 1.6.1. For the patients in the treatment group, a loading dose of dexmedetomidine will be given after induction of anaesthesia (1μg/kg over 10 min) followed by a continuous infusion (0.5μg/kg /h) until the end of surgery. 1.6.2. For patients in the placebo group, an equal volume loading dose of 0.9% saline will be given after the induction of anaesthesia followed by an equal volume continuous infusion until the end of surgery. 1.6.3. All other supplements, e.g. opioids, sedatives and muscle relaxant, will be identical in the both arms and administered according to routine clinical practice.
| Status | Completed |
| Enrollment | 330 |
| Est. completion date | December 31, 2022 |
| Est. primary completion date | October 31, 2022 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility | Inclusion Criteria: 1. Age 18-65 years 2. Scheduled to undergo allogenic liver transplant(DCD/DBD) surgery under general anaesthesia 3. Patients should meet the UCSF criteria 4. Agree to participate and give written informed consent Exclusion Criteria: 1. Severe renal dysfunction (undergoing renal replacement therapy before surgery) 2. Severe pulmonary dysfunction (including pneumonia, atelectasis, pleural effusion, acute lung injury or ARDS) 3. Severe circulatory instability (severe coronary artery disease, unstable angina, left ventricular ejection fraction < 30%, sick sinus syndrome, severe sinus bradycardia [< 50 bpm], second-degree or greater atrioventricular block) 4. Known allergy or intolerance to trial medication 5. Refusal to participate in the study 6. Participation in other clinical trials within 30 days prior to randomisation. 7. Retransplantation 8. Multiple organ transplantation 9. Other reasons that are considered unsuitable for study participation by the responsible surgeon or anaesthetist (reasons must be documented in the case report form [CRF]) |
| Country | Name | City | State |
|---|---|---|---|
| China | Renji Hospital, Shanghai Jiao Tong University, School of Medicine | Shanghai |
| Lead Sponsor | Collaborator |
|---|---|
| RenJi Hospital |
China,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Incidence of early allograft dysfunction (EAD) following surgery | Defined according to Olthoff's criteria published in 2010: (1) bilirubin = 10mg/dL on day 7; or (2) INR > 1.6 on day 7; or (3) AST/ ALT > 2000IU/L within first 7 days. | 7 days | |
| Secondary | Incidence of postoperative acute kidney injury (AKI) during the postoperative day 1-7 | Defined by Kidney Disease: Improving Global Outcomes (KDIGO) criteria published in 2012: (1) Increase in serum creatinine by = 0.3mg/dL within 48 hours; or (2) increase in serum creatinine to 1.5 times baseline or more within past 7 days; or (3) urine output < 0.5mL/kg/h for 6 hours. | 7 days | |
| Secondary | Incidence of acute respiratory distress syndrome (ARDS) during the postoperative day 1-7 | Defined according to Berlin modification of the American European Consensus Committee (AECC) definitions published in 2012: (1) Acute onset (within one week of known insult); and (2) bilateral opacities on CXR (not explained by effusions, nodules, or collapse); and (3) respiratory failure not fully explained by cardiac failure or fluid overload; and (4) Severity graded by PaO2/ FIO2 ratio with PEEP 5cmH2O i. Mild 300 = PaO2/ FIO2 > 200; ii. Moderate 200 = PaO2/ FIO2 > 100; iii. Severe 100 = PaO2/ FIO2. | 7 days | |
| Secondary | Incidence of graft failure and retransplantation rate during 3 year follow up period. | 3 years | ||
| Secondary | All cause mortality in the 3 year follow-up period. | 3 years | ||
| Secondary | Incidence of primary graft non-function (PNF) | Defined as graft loss, retransplantation, or patient death due to graft non-function in first 30 days (excluding non-function secondary to hepatic artery thrombosis, biliary complications, or recurrent hepatic disease). | 30 days |