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Pilot Study to Validate ex Vivo Expression of Specific Biomarkers of Human Resolutive Macrophages (RESOMACRO)

C

Centre Hospitalier Universitaire de Besancon

Status

Unknown

Conditions

Inflammation

Treatments

Procedure: blood sample or joint fluid or gingival exudate

Study type

Interventional

Funder types

Other

Identifiers

NCT05106075
2020/562

Details and patient eligibility

About

Human resolutive macrophages are essential immune cells in the resolution of inflammation. This particular type of macrophages remains poorly known and currently there are no biomarkers to identify them in vivo. Within UMR1098-RIGHT, specific biomarkers (secreted molecules and membrane receptors) of human resolutive macrophages (healthy volunteers) have been identified in vitro, but their existence in vivo remains an outstanding issue. An exploratory study (lack of data from the literature) will validate the ex vivo expression of these markers in samples of patients whose inflammation is not, or little, supported by the available therapies (NSAIDs, biotherapies, corticosteroids).

Enrollment

20 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age Limits (18-80 years)
  • Information and non-opposition for participating in the study
  • Patients suffering from periodontitis grade III ou IV
  • Patients suffering from microcristalline arthritis
  • patient with health insurance

Exclusion criteria

  • patient under corticotherapy
  • pregnancy
  • non-compliant patient
  • patient with no health insurance
  • patient in exclusion period from an other study
  • legal incapacity

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

biologic sample collection
Experimental group
Description:
Blood samples or gingival exsudat collection
Treatment:
Procedure: blood sample or joint fluid or gingival exudate

Trial contacts and locations

2

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Central trial contact

Thomas CHERRIER, MCU-PH

Data sourced from clinicaltrials.gov

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