Comparison of Inflammatory Profiles and Regenerative Potential in Alcoholic Liver Disease (TargetOH)
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| ClinicalTrials.gov Identifier: NCT03773887 |
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Recruitment Status :
Recruiting
First Posted : December 12, 2018
Last Update Posted : January 7, 2021
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Liver Diseases Acute on Chronic Hepatic Failure | Other: collection of liver biopsies collection of blood samples | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 450 participants |
| Allocation: | Non-Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Basic Science |
| Official Title: | Comparison of Inflammatory Profiles and Regenerative Potential in Alcoholic Liver Disease |
| Actual Study Start Date : | September 2015 |
| Estimated Primary Completion Date : | September 2027 |
| Estimated Study Completion Date : | September 2027 |
| Arm | Intervention/treatment |
|---|---|
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acute alcoholic hepatitis
collection of liver biopsies collection of blood samples in patients with acute alcoholic hepatitis (group A)
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Other: collection of liver biopsies collection of blood samples
blood and ascites samples; extraction of explants, hepatic resection parts; hepatic parenchyma on liver biopsies |
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Alcoholic cirrhosis
collection of liver biopsies collection of blood samples in patients with alcoholic cirrhosis (group B1)
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Other: collection of liver biopsies collection of blood samples
blood and ascites samples; extraction of explants, hepatic resection parts; hepatic parenchyma on liver biopsies |
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Without chronic liver disease
collection of liver biopsies collection of blood samples in patients without chronic liver disease (group B2)
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Other: collection of liver biopsies collection of blood samples
blood and ascites samples; extraction of explants, hepatic resection parts; hepatic parenchyma on liver biopsies |
- the expression of proinflammatory cytokines [ Time Frame: Baseline ]Proinflammatory Cytokines (TNF, IL-1, IL-6, IL-8)
- the expression of genetic variants of pro-inflammatory cytokines [ Time Frame: Baseline ]Identification of genetic variants of pro-inflammatory cytokines that contribute to mortality of Alcoholic Liver Disease
- Cell lysis (AST, ALT, CK18 cleaved) [ Time Frame: Baseline ]
- Regeneration markers (Ki-67, Fn14, CK7) [ Time Frame: Baseline ]
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| Ages Eligible for Study: | 18 Years to 70 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- group A: patients with acute alcoholic hepatitis
- Active alcohol abuse defined by DSM IV and excessive alcohol consumption prior to admission (> 60 g per day for men and> 40 g per day for women)
- Moderate elevation of transaminases (less than 500 U / L) with a typical ASAT / ALAT ratio of 2: 1
- Bilirubin> 50 mg / l
- Absence of autoimmune liver disease (ANA <1/80, AML <1/80, LKM1 neg, AAM neg)
- Absence of hepatitis B and C and HIV infection (negative anti-HIV antibodies, negative HBsAg, negative HCV PCR)
- Patients with other acute complications than alcoholic hepatitis may be included (eg, digestive hemorrhage, acute renal failure, infection, etc.)
- Because there is no validated noninvasive tool for the diagnosis of alcoholic hepatitis, histological confirmation is required in all patients (preferably by transjugular biopsy): alcoholic hepatitis will be diagnosed on the presence of the following histological characteristics: Hepatocellular lesions (ballooning, Mallory body)/ Inflammatory infiltrate with polymorphonuclear neutrophils
- group B1: patients with alcoholic cirrhosis
- Decompensated or non-decompensated alcoholic cirrhosis, defined according to the HAS guidelines, ie by a liver biopsy or a cluster of clinico-biological arguments (www.has-sante.fr)
- group B2: patients free from chronic liver disease
- Justification of blood and liver sampling for the management of a pathology other than chronic liver disease (eg liver metastasis of digestive cancer occurring on healthy liver)
Exclusion Criteria:
- For groups A and B1:
- Patients with hepatocellular carcinoma of progressive non-hepatic cancer
- Presence of HBsAg
- Presence of anti-HCV antibodies by positive PCR
- Presence of antibodies to HIV 1 +2
- Pregnancy
- for group B2:
- Alcoholic liver disease
- Presence of HBsAg
- Presence of anti-HCV antibodies by positive PCR
- Presence of antibodies to HIV 1 +2
- Pregnancy
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03773887
| Contact: Philippe Mathurin, MD,PhD | 03 20 44 55 97 ext +33 | philippe.mathurin@chru-lille.fr |
| France | |
| Hôpital Claude Huriez, CHRU | Recruiting |
| Lille, France | |
| Principal Investigator: Philippe Mathruin, MD,PhD | |
| Sub-Investigator: Alexandre Louvet, MD,PhD | |
| Principal Investigator: | Philppe Mathurin, MD,PhD | University Hospital, Lille |
| Responsible Party: | University Hospital, Lille |
| ClinicalTrials.gov Identifier: | NCT03773887 |
| Other Study ID Numbers: |
2014_30 2014-A01452-45 ( Other Identifier: ID-RCB Number, ANSM ) |
| First Posted: | December 12, 2018 Key Record Dates |
| Last Update Posted: | January 7, 2021 |
| Last Verified: | January 2021 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Liver Diseases Liver Diseases, Alcoholic Liver Failure Hepatic Insufficiency Digestive System Diseases |
Alcohol-Induced Disorders Alcohol-Related Disorders Substance-Related Disorders Chemically-Induced Disorders |

