Low-dose Arginine-vasopressin Supplementation on Post-transplant Acute Kidney Injury After Liver Transplantation (AVENIR Trial)
Launched by ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS · Mar 27, 2024
Trial Information
Current as of August 21, 2025
Not yet recruiting
Keywords
ClinConnect Summary
The AVENIR Trial is studying whether a treatment called low-dose arginine-vasopressin can help reduce the risk of acute kidney injury (AKI) in patients after they undergo a liver transplant. AKI is a common complication after this surgery, and it can lead to long-term kidney problems. The researchers believe that arginine-vasopressin, a hormone that helps regulate blood pressure, might protect the kidneys during and after the transplant process.
To participate in this trial, you need to be an adult (18 years or older) scheduled for a liver transplant and able to provide informed consent. However, if you are in a medical emergency situation, have severe kidney disease, or are pregnant or breastfeeding, you won't be eligible. Participants will receive clear information about the study and will be closely monitored throughout the process. This trial is not yet recruiting participants, but it aims to find a safer way to manage kidney health after liver transplants, which could lead to better overall outcomes for patients.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age ≥ 18 years
- • Any adult patient with a scheduled liver transplantation
- • All participants will need to be given clear information about the study and give signed informed consent.
- • Person affiliated to the Social Security
- Exclusion Criteria:
- • Super-emergency for liver transplantation or fulminant hepatitis
- • Patient listed for or receiving simultaneous liver-kidney transplantation (SLKT)
- • Patients with end-stage renal disease (chronic eGFR \< 15 mL/min/1.73 m2 or requiring extra-renal purification before liver transplantation
- • Patient with epilepsy
- • Hypersensitivity to arginine-vasopressin and to its excipients
- • Patient refusal
- • Patients for whom it is impossible to give informed consent (language barrier)
- • Adults under guardianship or trusteeship, persons deprived of their liberty
- • Patient enrolled in another interventional clinical study
- • Pregnancy or breastfeeding
About Assistance Publique Hôpitaux De Paris
Assistance Publique - Hôpitaux de Paris (AP-HP) is a leading public hospital system in France, renowned for its commitment to healthcare excellence and innovative medical research. As a prominent clinical trial sponsor, AP-HP plays a pivotal role in advancing medical knowledge and improving patient care through rigorous scientific investigations across a wide range of therapeutic areas. With a focus on collaboration and interdisciplinary approaches, AP-HP leverages its extensive network of hospitals and expert clinicians to facilitate high-quality clinical trials that adhere to the highest ethical and regulatory standards, ultimately aiming to translate research findings into tangible health benefits for diverse patient populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Paris, , France
Patients applied
Trial Officials
Jacques DURANTEAU, Pr
Study Director
Département Anesthésie-Réanimation - Université Paris-Saclay Hospital Bicêtre - Paul Brousse
Gilles LEBUFFE, Pr
Principal Investigator
Service Anesthésie-Réanimation - CHU de Lille
Daniel EYRAUD, Pr
Principal Investigator
Service Anesthésie-Réanimation -APHP Pitié-Salpêtrière
Emmanuel WEISS, Pr
Principal Investigator
Service Anesthésie-Réanimation - APHP hôpital Beaujon
Antoine DEWITTE, Pr
Principal Investigator
Service Anesthésie-Réanimation -CHU de Bordeaux centre médicochirurgical Magellan hôpital Haut Lévêque
Baptiste LORDIER, Pr
Principal Investigator
Service Anesthésie-Réanimation -CHU de Strasbourg Hôpital de Hautepierre
Alice BLET, Pr
Principal Investigator
Service Anesthésie-Réanimation - Hôpital de la Croix Rousse
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported