Loading clinical trials...
Loading clinical trials...
This is a multicentre observational study with prospective and retrospective data collection and retrospective data collection and biological collection from patients with HBV/HDV co-infection.
This is an observatory for patients co-infected with hepatitis B and Delta viruses. Patients will be monitored according to the usual recommendations, depending on their status: * Patients who have never received specific treatment for hepatitis Delta (untreated or receiving treatment with peginterferon alpha 2a alone) will be monitored according to current recommendations, once every 6 months; * Patients treated or having been treated with a specific hepatitis Delta treatment will be monitored according to the compassionate access protocol or according to the recommendations of the AMM during treatment and according to routine follow-up after the end of treatment. Participation in research entails the following additional procedures for patients, for each line of treatment, where applicable: * Samples for the biobank, * Self-administered questionnaires. In addition, as sub-studies are planned on sub-groups of patients, these sub-studies may involve additional constraints/interventions
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
CHU of Angers
Angers, France
Centre Hospitalier de la région annécienne
Annecy, France
Avicenne Hospital - Hepatology
Bobigny, France
Avicenne Hospital
Bobigny, France
Haut Lévêque Hospital
Bordeaux, France
Estaing Hospital
Clermont-Ferrand, France
Beaujon Hospital
Clichy, France
Centre Hospitalier Intercommunal
Créteil, France
Henri Mondor Hospital
Créteil, France
Bocage Hospital
Dijon, France
Start Date
February 19, 2020
Primary Completion Date
December 31, 2027
Completion Date
June 30, 2028
Last Updated
February 5, 2025
800
ESTIMATED participants
Blood draw for the laboratory assessment
OTHER
Lead Sponsor
ANRS, Emerging Infectious Diseases
NCT06550622
NCT05922306
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05870969