- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02113059
Platelets in Liver Regeneration
"Involvement of Platelets and Platelet Derived Growth Factors in Postoperative Liver Regeneration, Liver Dysfunktion and Morbidity in Patients Undergoing Hepatectomy"
Study Overview
Status
Conditions
Detailed Description
The investigators could previously show that platelet derived growth factors like TSP-1 and 5-HT are of relevance in human liver regeneration. In this project the investigators aim to elucidate how platelets specifically release their granules. Indeed, while dense granules stored 5-HT induces proliferation of hepatocytes, alpha-granules stored TSP-1 reduces their proliferative potential. More importantly, various pro-proliferative growth factors as VEGF are also stored in alpha-granules. Therefore, a systemic reduction in platelet counts would reduce both, pro and anti-proliferative factors. A highly regulated granula release has been postulated to allow platelets to exert specific functions. In 2008, Italiano et al. presented convincing in vitro evidence that platelets store molecules in separate granules, which they are able to specifically release upon platelet activation. Furthermore, results by other groups support this finding.
It is the aim of this project to characterize platelet activation in patients with liver resection and determine if specific platelet activation profiles correlate with clinical outcome.
Project plan
Included patients:
A total of 40 patients undergoing hemihepatectomy will be included. Patients will be closely monitored perioperatively. Plasma, serum, platelet and tissue preparation will be performed as outlined below.
Hypothesis No. 1:
Circulating platelet activation markers increase after liver resection.
To confirm the investigators initial observation of specific granula release, platelet activation will be monitored during liver regeneration. In particular, the investigators will evaluate platelet activation markers during the perioperative period. In a descriptive manner, the investigators will identify perioperative fluctuations of platelet activation as a reflection of physiologic processes during liver regeneration. This should enable the investigators to elucidate the occurrence of platelet activation in the human setting, as it has been described in murine models. More importantly, the investigators analyses could identify potential treatment targets in patients with insufficient hepatic regeneration.
Hypothesis No. 2:
Intra platelet granula contents decrease after liver resection.
Bioactive molecules stored in platelet alpha granules (intra platelet - IP), will be evaluated during the perioperative period. As during serum preparation all platelets degranulate, IP levels of granula contents will be calculated by subtraction of plasma from serum growth factor values. Furthermore to confirm these calculated values, platelet extracts will be generated and comparatively analyzed for IP growth factor levels. The investigators will further be able to identify perioperative fluctuations of IP growth factors as a reflection of specific intrahepatic release during liver regeneration, by comparing blood samples prior and one day after liver resection.
Hypothesis No. 3:
Platelets are locally enriched and activated at the site of liver regeneration.
During the process of a classical hemihepatectomy, the portal vein of the tumor containing liver lobe is initially ligated before mobilization and dissection of the liver. The increase of portal pressure within the remaining liver after partial hepatectomy is believed to be the major inducer of liver regeneration. (37-40) To evaluate if platelets play a critical role during the process of initiation of liver regeneration, tissue specimens will be collected prior to portal vein ligation and one hour after portal vein ligation (at the time of initiation of liver regeneration)(study design is illustrated in figure 3). Liver specimens will then be comparatively analyzed for platelet adhesion and protein as well as mRNA expression.
To further evaluate the relevance of platelets in the tightly regulated process of liver regeneration, blood will be collected 1 hour after portal vein ligation. In particular, blood will be drawn from the portal vein (prior to the liver) and from a liver vein (after the liver). From these samples platelets will be isolated and the degree of activation will be evaluated (details see below). Furthermore, the content of IP growth factors and platelet extracts will be analyzed to reflect their intrahepatic release.
Hypothesis No. 4:
Perioperative platelet activation has an impact on postoperative outcome
The predictive potential of platelet activation markers and IP growth factors to identify patients with poor postoperative clinical outcome will be analyzed. As outcome parameters postoperative LD, morbidity or mortality will be evaluated. These analyses might identify markers to select patients that should not undergo hepatectomy but be better served with alternative treatments. Furthermore, potential treatment targets in patients with insufficient hepatic regeneration could be identified.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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-
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Vienna, Austria, 1090
- Recruiting
- Medical University Vienna
-
Contact:
- Patrick Starlinger
- Phone Number: 00431404005621
- Email: patrick.starlinger@meduniwien.ac.at
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Contact:
- Thomas Gruenberger
- Phone Number: 00431404005621
- Email: thomas.gruenberger@meduniwien.ac.at
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Vienna, Austria, 1030
- Recruiting
- Rudolfstiftung
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Contact:
- Thomas Gruenberger, MD
- Phone Number: (+43 1) 711 65 - 0
- Email: thomas.gruenberger@meduniwien.ac.at
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients undergoing elective hemihepatectomy
Exclusion Criteria:
- peroperative portal vein thrombosis
- age > 85
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Liver resection
Patients undergoing a hemihepatectomy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Validation of the role of platelets in the process of early liver regeneration in humans
Time Frame: 2 years
|
Preclinical studies have identified multiple platelet associated candidate molecules in the highly regulated process of liver regeneration.
Using a complex peri and intraoperative sampling schedule, we will try to validate the relevance of these molecules in the human setting.
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Postoperative liver dysfunction
Time Frame: 2 years
|
Association of peri and intraoperative blood and tissue parameters associated with postoperative liver dysfunction
|
2 years
|
Postoperative morbidity
Time Frame: 2 years
|
Association of peri and intraoperative blood and tissue parameters associated with postoperative morbidity
|
2 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Patrick Starlinger, MD, PhD, Medical University Vienna
- Principal Investigator: Alice Assinger, PhD, Medical University Vienna
Study record dates
Study Major Dates
Study Start
Primary Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PS-AS-TG-CB
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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