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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03976765
Other study ID # 35RC18_9723_RAC-TH
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 17, 2018
Est. completion date August 11, 2020

Study information

Verified date April 2021
Source Rennes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Monocentric, prospective study to evaluate 10 liver transplanted patients


Description:

The improvement of perioperative technics and the prevention of complications with immunosuppression allowed for the development with success of liver transplant. 1322 liver transplants occurred in 2016 in France to 806 in 2000. Centre Hospitalier Universitaire (CHU) of Rennes became a reference with 122 liver transplants in 2016 being the second liver transplant center in France. Early rehabilitation concept is a multidisciplinary approach (surgical, anesthetic…) that aims to reduce the length of hospital stay and peri operative morbidity/mortality. These programs have first been developed in colorectal surgery before extending to complicated surgery like cephalic duodeno-pancreatectomy or hepatectomy. There are poor data in the literature on early rehabilitation program in liver transplant.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date August 11, 2020
Est. primary completion date August 11, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient older than 18 years old - First liver transplant - Liver transplant alone - MELD (Model for End stage Liver Disease) score = 15 - CHILD-PUGH score = 8 if cirrhosis - Body Mass Index < 30 kg/m2 - No history of transplant nor immunosuppression - Absence of ascites nor hydrothorax drain - Absence of treatment for diabetes - Absence of renal insufficiency (glomerular filtration flow > 60 mL/min) - Family help at home Exclusion Criteria: - Cold ischemia time > 8 hours - Grafts from type III Maastricht - Super urgent liver transplantation - Perioperative blood transfusion > 4 packed red blood cells and/or 3 fresh frozen plasma - Arterial anastomosis in splenic artery, in aorta or in coeliac artery - Bilio-digestive anastomosis - Persons deprived of liberty - Pregnant or breastfeeding women

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Rehabilitation program
The patients follow different rehabilitation programs (surgery, anesthetic, post-operative). Hospital discharge is authorized only after validation of objective, clinical and para clinic criteria

Locations

Country Name City State
France CHU de Rennes Rennes

Sponsors (1)

Lead Sponsor Collaborator
Rennes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with an hospital discharge at day 7 Day 7
Secondary Number of patients readmission in the first month Month 1
Secondary Number of days of hospitalization during the first month (post-surgery and prehospitalization) Month 1
Secondary Number of death in the first month Month 1
Secondary Satisfaction of the patient in the first month Month 1
Secondary Number of surgery complications according to Dindo and Clavien classification during the first month Month 1
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