Clinical Trial Details
— Status: Not yet recruiting
Administrative data
| NCT number |
NCT05772585 |
| Other study ID # |
APHP221332 |
| Secondary ID |
|
| Status |
Not yet recruiting |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
March 2023 |
| Est. completion date |
October 2023 |
Study information
| Verified date |
March 2023 |
| Source |
Assistance Publique - Hôpitaux de Paris |
| Contact |
Nicolas WEISS, MD, PhD |
| Phone |
01 42 16 27 70 |
| Email |
nicolas.weiss[@]aphp.fr |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
Hepatic encephalopathy is a frequent complication of both acute liver failure (ALF) and
acute-on-chronic liver failure (ACLF) and could be responsible among other neurological
complications of residual impairment after liver transplantation. Specific metabolomic
studies have shed light into pathophysiology. Nevertheless, whether HE metabolomic
fingerprints differ between HE in ALF and HE in ACLF and their evolution after liver
transplantation (LT) is unknown.
The aim of our study is to analyse the metabolomic fingerprint in plasma of 2 different
groups of patients before and after LT:
- hospitalized patients with ALF and HE
- hospitalized patients with ACLF and HE We will analyse metabolomic results to explore if
there is any difference in metabolomic fingerprints between these 2 groups and if LT
modify the metabolomic fingerprint in plasma in these 2 groups and in the same way.
We will collect blood samples in these 2 groups on the day of HE occurring and then on day 1,
day 7 and day 30 (+/- 2 days) after LT. We aim to enroll 10 patients in ALF group and 20
patients in ACLF group.
Inclusion criteria are defined as age > 18 years, patient presenting with ALF (Synthetic
liver failure (INR > 1.5) with hepatic encephalopathy (grade 1-4 of West-Haven
classification), without pre-existing hepatopathy, HE beginning within <26 weeks) or ACLF (≥
grade 1 from CANONIC criteria), and clinical HE (grade 1-4 of West-Haven classification) on
the day of enrolment. Exclusion criteria are defined as age < 18 years, absence of HE, LT
without pre-existing HE, patients who already undergone a LT, legally protected person.
An EDTA blood sample will be collected, centrifuged and frozen on the day of enrolment, then
on day 1, day 7 and day 30 (+/- 2 days) after LT. Metabolomic analyses will be performed by
different techniques but especially with high resolution liquid phase mass spectrometry in
collaboration with CEA. Statistical analyses will be both univariate (Mann-Whitney or
Wilcoxon tests) and multivariate (with a classical and adapted method for metabolomic
studies: Partial Least-Squares Discriminant Analysis (PLS-DA)).
We expect to identify different metabolomic fingerprints between HE in both ALF and ACLF
patients as well as different kinetics for symptoms resolution after LT. The long-term
objective is to target the specific metabolic pathways for each group in order to allow
development of new targeted drugs against HE in these 2 different conditions.
Description:
Every patient admitted with hepatic encephalopathy and ALF or ACLF in Intensive Care Unit
(ICU) or hepatology unit in both hospitals of Rennes University Hospital and La
Pitié-Salpêtrière University Hospital will be screened by physicians for inclusion and
exclusion criteria. If patients meet the criteria, their non-opposition of that of their
next-of-kin (in case of disturbed neurological state) will be collected and an information
paper will be given to them and their inclusion will be written in their medical file. On the
same day (Day 0), a 6mL EDTA tube will be collected during a blood sample included in the
standard patient care. Biological and demographic data collection will be done on day 0 too.
Then, patients will be followed-up during all the study duration and in case of LT, blood
sample with 6mL EDTA tube will be collected on day 1, 7 and 30 after LT. Data collection will
be performed at the time of each blood collection.
In case of the patient is not in hospital on the scheduled day, the blood collection will be
performed on the very next outpatient consultation.
Every blood sample will be included as part of the blood samples for standard patient care
and will under no circumstances be subject to a dedicated collection if the patient does not
benefit from a test on the scheduled day.
If patient did not underwent LT during the follow-up, then only day 0 blood sample will be
analyzed.
The blood samples will be centrifuged at 3000g for 10 min at 4°C, then the plasma will be
collected and aliquoted in 4 Eppendorf with 400µL of plasma in each. All the aliquots will be
stored at -80°C in the laboratories of the 2 centers.
After enrollment of the 30 expected patients, a secure transport network will be set up
between the laboratories of the Rennes University Hospital and the Pitié-Salpêtrière
University Hospital to the "Laboratoire d'Études du Métabolisme des Médicaments" of the CEA
Saclay Center.
Processing and metabolomic analysis will be carried out in the CEA laboratory. These analyses
will last approximately 2 weeks.
After having performed metabolites extraction in all the samples, high resolution liquid
phase mass spectrometry will be done.
Finally, data analyses will be done with the CEA team and the manuscript will be written at
the end of the study.
