The Effect of Remote Ischemic Preconditioning in Patients Undergoing Major Liver Surgery
Primary Purpose
Ischemia Reperfusion Injury
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
remote preconditioning
Sponsored by
About this trial
This is an interventional health services research trial for Ischemia Reperfusion Injury focused on measuring preconditioning, remote
Eligibility Criteria
Inclusion Criteria:
- Patients above the age of 18 undergoing liver surgery
Exclusion Criteria:
- Absence of written, informed consent.
- Patients with symptomatic peripheral vascular disease and absent or weak peripheral pulses.
- Patients with varicose veins and venous ulcers
- Patients with blood disorders, eg. sickle cell disease
- Patients with any localised limb infections eg. cellulitis
- Pregnancy
- HIV infection
- Fulminant sepsis
- Severe comorbid disease
- Patients below the age of 18
Sites / Locations
- Royal Free Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Other
Arm Label
Control group
RIPC
Arm Description
Patients undergoing liver surgery without the designated intervention
application of pneumatic tourniquet in patients undergoing liver surgery
Outcomes
Primary Outcome Measures
Does RIPC reduce ischemia reperfusion injury in patients undergoing liver surgery
Secondary Outcome Measures
Changes in liver regeneration
Full Information
NCT ID
NCT00796588
First Posted
November 21, 2008
Last Updated
November 21, 2008
Sponsor
Royal Free Hampstead NHS Trust
1. Study Identification
Unique Protocol Identification Number
NCT00796588
Brief Title
The Effect of Remote Ischemic Preconditioning in Patients Undergoing Major Liver Surgery
Official Title
The Effect of Remote Ischemic Preconditioning in Patients Undergoing Major Liver Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
November 2008
Overall Recruitment Status
Unknown status
Study Start Date
April 2005 (undefined)
Primary Completion Date
December 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Royal Free Hampstead NHS Trust
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The project has been designed to determine whether a brief period of leg ischemia will reduce the I/R injury sustained by the liver during liver surgery and liver transplantation. Adult patients (aged above 18) for liver resection (LR group) and for orthotopic liver transplantation (OLT group) will be analysed separately. Patients from each category will be randomised to two groups - a control and a Remote IPC group. In the remote IPC group Ischemic preconditioning will be induced during surgery by applying a pneumatic tourniquet to the upper part of the right thigh and then inflating it to twice the measured systolic arterial pressure in order to occlude the blood supply of the leg for 10 minutes. The tourniquet will then be deflated for 10 minutes to reperfuse the leg. This is repeated thrice to precondition the skeletal muscles of the leg.
Detailed Description
Data Collection & Measurements:
Blood Measurements: Blood will be collected at seven different time points, Baseline, Post IPC, 15 and 90 minutes post IRI and then 6,12 and 24 hours post IRI. At each time point approximately 35 ml of blood will be collected. Samples will be collected for the following measurements: Serum LFT and electrolytes, Serum CPK isozymes, Plasma cytokines, coagulation profile, TEG profile, Plasma cytokines, xanthine and XO/XDH activities, Plasma neutrophil activation, Total plasma Nitrate levels, Plasma lactate and ammonia levels and pulmonary artery blood (from indwelling Swan Ganz) for Plasma Myeloperoxidase levels. Some of these are routine measurements done during and after liver surgery.
Biopsies: Two Liver trucut biopsies - one prior to implantation (and in case of liver resection from the normal remnant liver before occlusion) and the other immediately prior to closure of the abdomen - will be taken to study the changes in tissue oxidation, tissue adhesion molecule upregulation and morphology prior to and after preconditioning.
Intra-operative haemodynamcis: Cardio-pulmonary haemodynamics will be monitored using a Swan-Ganz catheter (if it is clinically indicated and already in place) to note the effects of skeletal muscle ischemic preconditioning on the liver, lungs and the heart. In those patients undergoing liver resection invasive heaemodynamic monitoring will not be performed for the purpose of the study, if not required clinically by the anaesthetists and intensive care physicians. Non-invasive measurements will be made of hepatic and cutaneous circulation using surface Laser Doppler flow meter and Ultra sound probes. Cutaneous microvascular responses to iontophoresis (non-invasive) of acetylcholine, an endothelium-independent vasodilator and sodium nitroprusside, and endothelium-independent vasodilator will be measured using the laser Doppler flow meter. NIRS probes (non -invasive) will be used on the surface of the to measure liver tissue oxygenation. All probes will be properly sterilised prior to application.
Post-operative heamodynamics: Cardio-pulmonary haemodynamics will continue to be monitored using a Swan-Ganz catheter (routinely inserted during liver transplantation) in the post-operative period for 24 hours.
ICG measurements: To assess liver function by injecting 0.5 mg/kg of indocyanine green (ICG) pre-operatively, intra-operatively and post operatively. ICG is routinely used in many liver centres for the assessment of liver function in clinical practise. No additional blood samples will be collected since the uptake and excretion of ICG by the liver will be measured by a non invasive digital pulse densitometric device (ICG Pulsion) connected to the patient by a finger sensor.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemia Reperfusion Injury
Keywords
preconditioning, remote
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
48 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients undergoing liver surgery without the designated intervention
Arm Title
RIPC
Arm Type
Other
Arm Description
application of pneumatic tourniquet in patients undergoing liver surgery
Intervention Type
Other
Intervention Name(s)
remote preconditioning
Other Intervention Name(s)
RIPC
Intervention Description
Three periods of 10 minute occlusion of blood supply to leg using a pneumatic tourniquet
Primary Outcome Measure Information:
Title
Does RIPC reduce ischemia reperfusion injury in patients undergoing liver surgery
Time Frame
8 years
Secondary Outcome Measure Information:
Title
Changes in liver regeneration
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients above the age of 18 undergoing liver surgery
Exclusion Criteria:
Absence of written, informed consent.
Patients with symptomatic peripheral vascular disease and absent or weak peripheral pulses.
Patients with varicose veins and venous ulcers
Patients with blood disorders, eg. sickle cell disease
Patients with any localised limb infections eg. cellulitis
Pregnancy
HIV infection
Fulminant sepsis
Severe comorbid disease
Patients below the age of 18
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian R Davidson, FRCS, MD
Organizational Affiliation
Royal Free Hospital and medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Free Hospital
City
London
ZIP/Postal Code
NW3 2QG
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
18456674
Citation
Hausenloy DJ, Yellon DM. Remote ischaemic preconditioning: underlying mechanisms and clinical application. Cardiovasc Res. 2008 Aug 1;79(3):377-86. doi: 10.1093/cvr/cvn114. Epub 2008 May 2.
Results Reference
background
PubMed Identifier
27054029
Citation
Robertson FP, Goswami R, Wright GP, Fuller B, Davidson BR. Protocol for a prospective randomized controlled trial of recipient remote ischaemic preconditioning in orthotopic liver transplantation (RIPCOLT trial). Transplant Res. 2016 Apr 6;5:4. doi: 10.1186/s13737-016-0033-4. eCollection 2016.
Results Reference
derived
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The Effect of Remote Ischemic Preconditioning in Patients Undergoing Major Liver Surgery
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