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Blood clotting in the portal vein and body of people with cirrhosis

Compares blood clotting in the portal vein and body in cirrhosis patients.

Plain-language title generated from the registry record
Registry title: Exploration of Systemic and Portal Hemostasis in Patients Undergoing Transjugular Intrahepatic Portosystemic Shunt Placement

Key facts

Where
Villejuif, FranceSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with cirrhosis who are followed at Paul Brousse Hospital and are having a TIPS (transjugular intrahepatic portosystemic shunt) placed.

Age
18 years or older
Sex
All sexes
Disease stage
Cirrhosis, with a TIPS placement planned
Earlier treatment
Treatment that affects blood clotting must have been stopped for the procedure. No systemic corticosteroid treatment.

Main reasons for not taking part

  • Unwilling to take part
  • Cannot have a TIPS placed (contraindication)
  • Known clotting disorder not caused by cirrhosis
  • Taking treatment that affects clotting and not stopped for the procedure
  • Taking systemic corticosteroids

Read by machine on 13 November 2026.

Where in France

  • Hôpital Paul-BrousseVillejuif, FranceContact: STEPHANIE ROULLET, PhDTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
Assistance Publique - Hôpitaux de Paris
Trial code
NCT07439939
Record updated
21 April 2026
Original description
Portal vein thrombosis is defined as non-tumoural obstruction of the portal vein or one of its branches. Its incidence is 0.7 to 2.7 per 100,000 patient-years in the general population, and 4.6 per 100 patient-years in patients with cirrhosis. Histological modificaitions fo the portal vein wall and haemostatic changes have been described in cirrhotic patients. The contribution of these changes, both systemic and local, to the development of portal vein thrombosis is debated. One of the hypotheses put forward on the genesis of portal vein thrombosis is as follows: certain bacterial translocations from the digestive tract, promoted by portal hypertension, contribute to endothelial activation resulting in the release of von Willebrand factor and factor VIII, as well as platelet activation and the coagulation cascade, which is dysregulated by cirrhosis and underlying changes in haemostatic balance. Inflammatory phenomena and NETosis may also be involved. Studies suggest that cirrhotic patients have lesions of the glycocalyx located in the portal area, which may be involved in the development of portal vein thrombosis. Patients with cirrhosis may benefit from the placement of a transjugular intrahepatic portosystemic shunt (TIPS). During the TIPS placement procedure, blood is drawn from the internal jugular vein and the portal vein, allowing for parallel biological analyses. The assumption of this study is that haemostasis and inflammation are disrupted differently at the systemic and portal levels in cirrhotic patients.Read full original descriptionShow less

Exploration of Systemic and Portal Hemostasis in Patients Undergoing Transjugular Intrahepatic Portosystemic Shunt Placement

Portal vein thrombosis is defined as non-tumoural obstruction of the portal vein or one of its branches. Its incidence is 0.7 to 2.7 per 100,000 patient-years in the general population, and 4.6 per 100 patient-years in patients with cirrhosis. Histological modificaitions fo the portal vein wall and haemostatic changes have been described in cirrhotic patients. The contribution of these changes, both systemic and local, to the development of portal vein thrombosis is debated. One of the hypotheses put forward on the genesis of portal vein thrombosis is as follows: certain bacterial translocations from the digestive tract, promoted by portal hypertension, contribute to endothelial activation resulting in the release of von Willebrand factor and factor VIII, as well as platelet activation and the coagulation cascade, which is dysregulated by cirrhosis and underlying changes in haemostatic balance. Inflammatory phenomena and NETosis may also be involved. Studies suggest that cirrhotic patients have lesions of the glycocalyx located in the portal area, which may be involved in the development of portal vein thrombosis. Patients with cirrhosis may benefit from the placement of a transjugular intrahepatic portosystemic shunt (TIPS). During the TIPS placement procedure, blood is drawn from the internal jugular vein and the portal vein, allowing for parallel biological analyses. The assumption of this study is that haemostasis and inflammation are disrupted differently at the systemic and portal levels in cirrhotic patients.

Inclusion: Adult patients (aged ≥18 years) covered by a social security scheme or entitled beneficiaries; Patients followed for a cirrhotic condition at Paul Brousse Hospital and undergoing placement of a TIPS (transjugular intrahepatic portosystemic shunt).

Exclusion: Patient receiving treatment that interferes with hemostasis and has not been discontinued for the procedure; Patient receiving systemic corticosteroid therapy; Patient with a known hemostatic disorder unrelated to cirrhosis; Patient unwilling to participate in the study; Patient with a contraindication to TIPS placement; Patient under legal protection; Patient not covered by a social security scheme.

ClinicalTrials.gov NCT07439939