- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03762876
Evaluation of Trans-Hepatic Flow Changes in Major Hepatectomy (THEFLOW)
Evaluation of Trans-Hepatic Flow Changes in Major Hepatectomy-THEFLOW Study
Changes in trans-hepatic flow after major and extended hepatectomy (EH) can lead to small for size and flow syndrome (SFSF), which is associated with a significantly higher rate of morbidity and mortality. The current therapies for SFSF are not effective because tissue damage following SFSF is usually irreversible and the liver parenchyma loses the ability to regenerate. Therefore, the best approach to improve patient survival is to predict SFSF and perform adequate intraoperative preventive procedures.
Portal vein flow (PVF), hepatic artery flow (HAF), and portal vein pressure (PVP) are the main criteria for development of SFSF after living donor liver transplantation. The mechanisms that change trans-hepatic flow are similar after hepatectomy and living donor liver transplantation. Trans-hepatic flow is routinely measured during liver resection, but the effect of these changes on SFSF has not been studied. Identifying the factors that alter trans-hepatic flow after hepatectomy would allow hepatic inflow to be modulated before and after surgery, to prevent SFSF.
Trans-hepatic flow and pressure parameters (PVF, HAF, and PVP) are routinely measured and monitored during liver resection. The aim of the proposed study is to analyze changes in these parameters after major hepatectomy and determine the factors that alter trans-hepatic flow after hepatectomy.
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiesteder
-
-
Baden-Württemberg
-
Heidelberg, Baden-Württemberg, Tyskland, 69120
- Rekruttering
- Division of Visceral Transplantation, Department of General, Visceral and Transplantation Surgery, University of Heidelberg
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Patient consent
- Undergoing major or central liver resection
- Aged above 18 years
Exclusion Criteria:
- Cirrhosis
- Previous surgery of the hepatoduodenal ligament
- Status after transjugular intrahepatic portosystemic shunt
- Metabolic liver diseases
- Cardiac failure
- Pulmonary hypertension
- Portal vein thrombosis
- Portal vein hypertension
- Vascular malformation
- Not able to give consent
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Portal vein flow
Tidsramme: One day
|
One day
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Sygelighedsrate
Tidsramme: Tre måneder
|
Baseret på Clavien-Dindo klassifikationen
|
Tre måneder
|
|
Dødelighedsrate
Tidsramme: Tre måneder
|
Alle forårsager dødsbegivenheder
|
Tre måneder
|
|
Portal vein pressure
Tidsramme: One day
|
Vein pressure (mmHg)
|
One day
|
|
Hepatic artery flow
Tidsramme: One day
|
One day
|
|
|
Central vein pressure
Tidsramme: One day
|
Vein pressure (mmHg)
|
One day
|
|
Mean arterial pressure
Tidsramme: One day
|
One day
|
|
|
Post-hepatectomy liver failure
Tidsramme: Three months
|
Based on the ISGLS criteria
|
Three months
|
|
Grade of liver stiffness
Tidsramme: Three months
|
Via fibroscan before and after resection
|
Three months
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Mohammad Golriz, MD, Department of General, Visceral and Transplant Surgery, University Hospital
- Studieleder: Arianeb Mehrabi, MD, Department of General, Visceral and Transplant Surgery, University Hospital
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- S-576/2017
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Større hepatektomi
-
Tonix Pharmaceuticals, Inc.RekrutteringDepression | Major Depressive Disorder (MDD) | Major Depressive Episode (MDE)Forenede Stater
-
University of PretoriaIkke rekrutterer endnuMajor Depressive Disorder (MDD)Saudi Arabien
-
Tel Aviv UniversityIkke rekrutterer endnuMajor Depressive Disorder (MDD)Israel
-
Instituto Mexicano del Seguro SocialAfsluttet
-
Yonggui YuanIkke rekrutterer endnuMajor Depressive Disorder (MDD)Kina
-
Daniel LindqvistLund University; KetabonRekrutteringMajor Depressive Disorder (MDD)Sverige
-
King's College LondonCardiff and Vale University Health Board; South London and Maudsley NHS... og andre samarbejdspartnereRekrutteringMajor Depressive Disorder (MDD)Det Forenede Kongerige
-
Supernus Pharmaceuticals, Inc.RekrutteringMajor Depressive Disorder (MDD)Forenede Stater
-
University of PennsylvaniaRekruttering
-
The Second Hospital of Anhui Medical UniversityIkke rekrutterer endnu