Role of Gut Microbiota in the Pathophysiology of Aseptic Abscesses
Launched by UNIVERSITY HOSPITAL, CLERMONT-FERRAND · Sep 8, 2022
Trial Information
Current as of July 12, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a rare condition called aseptic abscess syndrome (AA), where patients develop deep abscesses—painful lumps filled with pus—without any bacteria found in their bodies. Since antibiotics don’t work for this condition, doctors often use anti-inflammatory medications like corticosteroids to help patients feel better. The researchers want to learn more about the role of gut bacteria in this syndrome, especially since gut health is important for our immune system. They will collect samples from patients and healthy individuals to see if there are differences in gut bacteria and other biological markers related to AA.
To participate in this trial, adults aged 65 to 74 who have been diagnosed with aseptic abscess syndrome may be eligible if they have certain signs of the condition, such as deep abscesses that have been examined through imaging and lab tests showing no infection. Participants will need to be able to give consent and be part of the Social Security system. Those living with the patient, such as family members or close contacts, may also participate as healthy controls. Throughout the study, participants can expect to provide stool, blood, saliva, and urine samples, which will help researchers understand the link between gut bacteria and this syndrome.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- * For cases: adult patients meeting the diagnostic criteria for aseptic abscess syndrome described by André et al:
- • Deep abscesses on radiological examination with neutrophilic features proven by pathological analysis of a surgical specimen or biopsy when performed
- • Negative blood cultures, negative serological tests for bacteria, including always Yersinia enterocolitica, and, during surgery or aspiration, sterile pus (with standard cultures, BAAR and fungal tests) Failure of antibiotic therapy, when prescribed, after at least 2 weeks for conventional antibiotic therapy and at least 3 months for anti-tuberculosis treatment
- • Rapid clinical improvement the day after the prescription of corticosteroids (at least 1/2 mg/kg prednisone or equivalent) followed by radiological improvement after 1 month of corticosteroids, sometimes in association with immunosuppressive treatments.
- • For controls: adult person living in the same environment as the case to which it is matched. Adult person living in the same household or near the patient.
- For cases and controls:
- • Ability to provide informed consent.
- • Membership in the Social Security system.
- Exclusion Criteria:
- • Pregnant women. Incapable patients Patients deprived of liberty Antibiotic therapy administered within 6 weeks prior to inclusion.
About University Hospital, Clermont Ferrand
The University Hospital of Clermont-Ferrand is a leading academic medical institution dedicated to advancing healthcare through innovative research and clinical trials. Renowned for its multidisciplinary approach, the hospital integrates cutting-edge scientific inquiry with patient care, fostering an environment that promotes collaboration among healthcare professionals, researchers, and academic partners. With a strong commitment to improving patient outcomes, the institution actively engages in a wide array of clinical studies, ranging from early-phase trials to large-scale interventions, aimed at addressing critical health challenges and enhancing treatment modalities. Its state-of-the-art facilities and expertise make it a pivotal contributor to clinical research in the region and beyond.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Dax, , France
Nantes, , France
Bordeaux, , France
Clermont Ferrand, , France
Lyon, , France
Montpellier, , France
Nîmes, , France
Charleville Mézières, , France
Créteil, , France
Lyon, , France
Marseille, , France
Paris, , France
Paris, , France
Paris, , France
Paris, , France
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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