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Liver Transplantation clinical trials

View clinical trials related to Liver Transplantation.

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NCT ID: NCT04945135 Completed - Liver Transplant Clinical Trials

Controlled Donors After Circulatory Death and Brain Death: a Multicenter Study of Transfusion, One-year Graft Survival and Mortality. Cohort Study,

Start date: June 1, 2019
Phase:
Study type: Observational

RBC requirement ein DBD and DCD liver transplants

NCT ID: NCT04941911 Active, not recruiting - Clinical trials for Liver Transplantation

A Feasibility Study of Octreotide Infusion During Liver Transplant.

Octreotide
Start date: May 27, 2022
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether an octreotide infusion during liver transplantation improves renal outcomes, intraoperative blood pressure and reduces haemorrhage and transfusion requirement.

NCT ID: NCT04925843 Completed - Clinical trials for Liver Transplant; Complications

Fibrinogen and Intraoperative Bleeding in Liver Transplant

FIB_TOF
Start date: July 15, 2019
Phase:
Study type: Observational

Liver transplantation is the only treatment for end-stage liver disease. It is a high-risk surgery that can cause heavy intraoperative bleeding. Bleeding and transfusions of blood products are themselves associated with several postoperative complications. Few data have suggested beneficial interventions that can decrease this bleeding. Such interventions are necessary in order to improve these patients' outcomes. In order to better understand the potential therapeutic targets, a better comprehension of the variables associated with such bleeding is essential. Several previous studies have demonstrated a weak association between usual clotting times and bleeding in this population. However, few studies have evaluated the association between the concentration of fibrinogen and bleeding in this population. The primary objective of this study is to assess the association between preoperative serum fibrinogen concentration and the volume of intraoperative bleeding. The secondary objective is to assess the association between preoperative serum fibrinogen concentration and the number of red blood cell units transfused during the intraoperative and immediate postoperative periods. The hypothesis of the study is that a low concentration of preoperative fibrinogen will be associated with an increase in intraoperative bleeding and red blood cell transfusions.

NCT ID: NCT04901169 Recruiting - Clinical trials for Liver Transplant; Complications

Angiotensin II in Liver Transplantation

AngLT-1
Start date: June 28, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of Angiotensin II as a second-line vasopressor (drug that raises the blood pressure) during liver transplantation.

NCT ID: NCT04885582 Completed - Clinical trials for Liver Transplant; Complications

The Relationship Between HLA Tissue Compatibility and Biliary Complications in Patients With Liver Transplantation

Start date: May 10, 2017
Phase:
Study type: Observational

Liver transplantation has become the accepted treatment option for advanced liver failure in recent years. In addition to the increase in the number of centers performing transplant and the decrease in complication rates depending on the experience gained, the most common biliary complications did not improve at the desired level. For this reason, studies in this field are frequent today. The structural complexities of HLA antigens have been the subject of investigation in recent years. With the development of DNA and RNA amplification methods; It is increasingly difficult for physicians to keep up with the increasing burden of knowledge regarding the genetic aspects of these antigens. Concrete benefits of this gene complex, which has been investigated in various fields and preserves its mystery, have not been determined in liver transplant patients. However, there are publications showing its connection with the bile epithelium in liver transplantation and its relationship with the disappearing bile duct syndrome. In this study, our aim is to explain whether the bile duct complications, which appear like a continuous wall and can lead to frightening pictures, are related to HLA tissue compatibility.

NCT ID: NCT04867720 Recruiting - Liver Transplant Clinical Trials

Efficacy and Safety of CertiroBell® Tablet Plus Tacrolimus in Primary Living Donor Liver Transplant Recipients

STELLA
Start date: March 16, 2021
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy and safety of CertiroBell® tablet plus tacrolimus

NCT ID: NCT04862156 Terminated - Clinical trials for Liver Transplantation

WP02 Continued Access Study

Start date: October 10, 2021
Phase: N/A
Study type: Interventional

The single-arm continued access phase will be used to collect additional effectiveness and safety data to support the objectives and outcomes of the original IDE pivotal study.

NCT ID: NCT04854564 Completed - Clinical trials for Liver Transplant; Complications

Identifying Perceived Barriers and Facilitators Toward a Liver Transplantation Prehabilitation

Start date: August 1, 2021
Phase:
Study type: Observational

The purpose of this study is to formally identify patient and caregiver perceived needs, barriers, and facilitators to inform the development of a home-based multimodal prehabilitation program for potential LT candidates.

NCT ID: NCT04853641 Completed - Clinical trials for Perioperative/Postoperative Complications

Impact of Age and BMI on Liver Transplant Outcomes

Start date: July 1, 2020
Phase:
Study type: Observational

Prospectively enrolled retrospective chart review and Liver Transplant database review to determine the modifiable and nonmodifiable risk factors specifically relating to Living Donor Liver Transplants. To observe the impact of age and BMI on graft outcomes and whether they impact the intraoperative management, post-operative length of stay, and complications.

NCT ID: NCT04838314 Terminated - Clinical trials for Liver Transplant Disorder

Perioperative Analgesia by ESP Catheter on Paediatric Recipient for Liver Transplantation

ESPLIVPAED
Start date: June 1, 2021
Phase: N/A
Study type: Interventional

Pediatric Liver transplantation surgery is associated with moderate to severe postoperative pain that is related to large abdominal incision cutting muscles and fascia and the anterior abdominal wall and drains. Peri-operative pain management after this surgery is centered on intravenous opioids, which cannot provide complete pain relief and are responsible for side effects such as vomiting or respiratory depression. Fifty-two per cent of pediatric patients reported moderate to severe pain on the day of surgery and 33% on day 1. 42% of patients reported vomiting. Increasing interest has focused on opioid sparing analgesic strategies to avoid some of the detrimental side effects of opioids. Recently, the focus has been on postoperative regional analgesia after major pediatric in major thoracic or abdominal surgeries. Thoracic epidural anesthesia or paravertebral blocks are efficacious but raise some concerns related to their potential complications especially in Liver transplantation with the risk of coagulation disorders. Erector spinae plane block (ESPB) is an interfascial plane block whereby Local anesthestic (LA) is injected beneath the iliocostalis, longissimus, and spinalis muscles to achieve multi metameric analgesia for pediatric thoracic, cardiac, or abdominal surgery. I Investigators' hypothesis is with efficient peri operative regional analgesia will reduce the opioids consumption, allow a very early extubation after such long surgeries and improve the quality of recovery by reducing the side effects of opioids as sedation. nausea vomiting delay of first intake.