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| Name | Class |
|---|---|
| Sahlgrenska University Hospital | OTHER |
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Evaluating hemostasis in decompensated liver cirrhosis with novel hemostatic assays.
The rebalanced hemostasis in liver cirrhosis is vulnerable and patients are prone to both bleeding and thrombosis. There are today no gold standard for evaluating the hemostasis and we will evaluate novel methods for this.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Non-acute decompensated liver círrhosis | Refractory ascites, low grade encephalopathy but manages to stay at home and only come in ofr check-ups. |
| |
| Acute decompensated liver cirrhosis | Acute event causing further decompensation and the need for in-patient care |
| |
| Acute on chronic liver failure | ACLF 1-3 accordic to criterias established through the Cannonic study. |
| |
| Controls | Healthy individuals |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| T-TAS | Diagnostic Test | Blood test, laboratory assays |
|
| Measure | Description | Time Frame |
|---|---|---|
| Differences in laboratory values between groupstests | Laboratory values of novel hemostasis tests TTAS, Quantra and OHP correlated to Rotem, TG and conventional coagulation assays. All tests have differnet values. | up to 5 years |
| Correlation between systemic inflammation and hemostasis measured by novel assays | Correlation between systemic inflammation measured by cytokines, NETs and ECV and hemostasis measured by novel assays as in outcome 1 | uo to 7 years |
| Measure | Description | Time Frame |
|---|---|---|
| Number of participant with bleeding | Bleeding defined according to ISTH | Up to 7 years |
| Number of participants with Thrombosis | Splanchnic or non-splanchnic thrombosis |
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Inclusion Criteria:
Exclusion Criteria:
• Extrahepatic malignancy or recurrence of such within the last year.
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40 patients each with NAD, AD and ACF and 30 healthy volunteers.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sanna Norén, MD, PhDstudent | Contact | +46703131799 | sanna.noren@regionstockholm.se | |
| Maria Magnusson, MD, PhD | Contact | maria.s.magnusson@regionstockholm.se |
| Name | Affiliation | Role |
|---|---|---|
| Maria Magnusson, MD, PhD | Region Stockholm, Karolinska Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Karolinska University Hospital | Recruiting | Stockholm | Huddinge | 14186 | Sweden |
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Hemostasis assays, inflammation assays, DNA
|
| Up to 7 years |
| Number of participants that die | Up to 7 years |
| Number of participant going to transplant | Number of patients getting a transplant, acute, subacute or according to waiting list | Up to 7 years |