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The Effects Of Remote Organ Ischemic Preconditioning On Systemic Inflammatory And Glycocalyx Integrity Parameters

The Effects Of Remote Organ Ischemic Preconditioning On Systemic Inflammatory And Glycocalyx Integrity Parameters In Living-Donor Liver Transplantation Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04216407
Enrollment
22
Registered
2020-01-02
Start date
2019-12-05
Completion date
2020-03-20
Last updated
2020-04-08

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

Conditions

Remote Organ Ischemic Preconditioning

Keywords

Remote organ ischemic preconditioning, Ischemia reperfusion injury, Glycocalyx integrity parameters, Systemic inflammation parameters

Brief summary

Ischemia-reperfusion (IR) injury during liver transplantation is one of the major causes of mortality and morbidity associated with transplantation. Remote organ ischemic preconditioning (RIPC) is one of the most investigated practices to reduce IR injury. In this study, for the first time in the clinic, the effect of RIPC will be evaluated via both systemic inflammation parameters and also parameters showing glycocalyx integrity, on living-donor liver recipients.

Interventions

PROCEDURERemote ischemic preconditioning

An orthopedic tourniquet was tied to the right lower extremities of the patients in RIPC arm, and tourniquet application was performed before the anhepatic phase in 3 periods of 3 minutes with an interval of 3 minutes.

Sponsors

Acibadem University
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Patients followed up by Acıbadem Hospital Organ Transplantation Center * Patients accepted to participate in the study * Older than 18 years of age * ASA class III * MELD score \>12 * Scheduled for elective liver transplantation surgery from a living donor

Exclusion criteria

* Patients undergoing re-transplantation * Under the age of 18 years * Patients undergoing emergency surgery * Patients with hepatorenal or hepatopulmonary syndrome * Patients receiving mechanical ventilation support in the ICU * Patients refusing to participate

Design outcomes

Primary

MeasureTime frameDescription
soluble Vascular cell adhesion molecule-1 (sVCAM-1).Postoperative early period (6 hours after intensive care unite admission)Evaluation of sVCAM-1 level difference between groups
Intercellular adhesion molecule-1 (ICAM-1)Postoperative early period (6 hours after intensive care unite admission)Evaluation of (ICAM-1) level difference between group
Hypoxia-induced factor-1 (HIF-1)Postoperative early period (6 hours after intensive care unite admission)Evaluation of HIF-1 level difference between groups
Interleukin-8 (IL-8)Postoperative early period (6 hours after intensive care unite admission)Evaluation of IL-8 level difference between groups
Syndecan-1 (SDC-1)Postoperative early period (6 hours after intensive care unite admission)Evaluation of SDC-1 level difference between groups
Tumor necrosis factor-alpha (TNF-alpha)Postoperative early period (6 hours after intensive care unite admission)Evaluation of TNF-alpha level difference between groups

Secondary

MeasureTime frameDescription
Liver function tests7 days after surgeryEvaluation of early postoperative liver function tests; AST and ALT
Length of stay in hospital and intensive care unit7 days after surgeryEvaluation of the length of stay in hospital and intensive care unit
Morbidity7 days after surgeryEarly postoperative complications
Mortality7 days after surgeryEarly postoperative mortality

Countries

Turkey (Türkiye)

Outcome results

None listed

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