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Clinical Trials/NCT06944873
NCT06944873Not yet recruitingNot Applicable

Metabolic Reprogramming of Monocytes in Inflammatory Flares of Inflammatory Bowel Diseases

University Hospital, Grenoble1 site in 1 country30 target enrollmentStarted: July 1, 2026Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Comparaison of reduction of concentration of inflammatory cytokines and chemokines in cells treated by oxygen microbubbles vs cells not treated

Study Overview

Brief Summary

Inflammatory bowel diseases, Crohn's disease and haemorrhagic rectocolitis, are pathologies that progress in flare-ups, impacting on patients' quality of life and functional or even vital prognosis. These inflammatory diseases require the use of immunosuppressive and immunomodulatory treatments, the side-effects of which can be significant, and the limited number of which sometimes puts patients and practitioners in a therapeutic impasse from which surgery is the only way out. It is therefore important to be able to develop new therapeutic approaches, ideally better tolerated, that can control inflammation during relapses. Monocytes are one of the main players in the inflammatory reaction. In the laboratory, we have developed a strategy for the metabolic reprogramming of these cells based on the use of oxygen microbubbles to modulate the inflammatory response of monocytes.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Men and women over 18
  • •Managed at the CHUGA for a severe IBD flare-up requiring hospitalisation or endoscopy for flare-up
  • •Patient not objecting to the REPRO-MICI study

Exclusion Criteria

  • •Patients protected by law (pregnant or breast-feeding women, minors, patients under guardianship or trusteeship, persons deprived of their liberty or hospitalised under duress).
  • •Patients with positive HIV, HBV or HCV serology.
  • •Patients with a positive ELISPOT with no history of treatment for latent tuberculosis.

Outcomes

Primary Outcomes

Comparaison of reduction of concentration of inflammatory cytokines and chemokines in cells treated by oxygen microbubbles vs cells not treated

Time Frame: up to 2 years

Validation of inhibition of the production of inflammatory cytokines and chemokines by the monocytes treated by oxygen microbubbles

Secondary Outcomes

  • Comparaison of glucose metabolism rate in monocytes treated bu microbubbles vs not treated cells(up to 2 years)
  • Comparaison of tissue factor expression at the membrane of monocytes treated by microbubbles vs monocytes not treated(up to 2 years)

Investigators

Sponsor
University Hospital, Grenoble
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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