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Not yet recruitingNCT07885501MUMIPUpdated Oct 21, 2026

The Microbiome in Uveitis and Pediatric Inflammatory Diseases

An observational study in Noninfectious Uveitis, sponsored by Assistance Publique - Hôpitaux de Paris. Not yet recruiting at 1 site in France. Open to participants aged 1 Day to 17 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by Assistance Publique - Hôpitaux de Paris · Observational

Updated Oct 21, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Ages
1 Day to 17 Years
Sex
All
01

Study summary

Chronic, noninfectious uveitis in children, associated with various systemic inflammatory diseases, carries a high risk of vision loss. Intestinal dysbiosis and the translocation of bacterial peptidoglycans (PG) that activate innate receptors recognizing PG could represent a common initiating mechanism, independent of the underlying disease. Studying these biological signatures in comparative cohorts could lead to a better understanding of the onset of uveitis and the development of targeted diagnostic and therapeutic strategies.

Read the detailed description

The objectives of this project are to characterize the peptidoglycan (PG) signature in healthy children and in the context of pediatric noninfectious uveitis; to compare the peptidoglycan signatures of patients with noninfectious uveitis to those with pediatric inflammatory diseases without uveitis; and to determine the correlation between these PG signatures, microbiota composition, and disease parameters in the context of uveitis.

Participants will be informed about the study during their routine follow-up visits.

  • A stool collection kit, containing all necessary supplies and instructions, will be provided to families.
  • Samples will be collected at the hospital or at home and then sent directly to the laboratory by mail.
  • For patients, blood samples collected as part of routine care (blood draws for routine laboratory tests) and of which a portion is not used will be collected to establish a biobank dedicated to research.

These procedures do not require any additional medical procedures or visits beyond routine follow-up.

02

Conditions studied

  • Noninfectious Uveitis

Keywords

  • pediatric inflammatory diseases without ocular involvement
  • gut microbiota
03

In context

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,576 studies on the registry; 1,028 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Day to 17 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

  • Confirmed infectious uveitis (bacterial, viral, fungal, parasitic)
  • Participation in an interventional clinical trial affecting the microbiome or immune system

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients under the age of 18 being treated at Robert-Debré Hospital
  • Patients being treated for noninfectious uveitis, or with pediatric inflammatory diseases without uveitis (connective tissue disorders, granulomatosis, juvenile idiopathic arthritis, pediatric vasculitides).
  • The child and his or her parents have no objection to participating in the study
  • Siblings of patients (family controls) or other healthy controls (children of hospital staff)

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes
Biospecimen retention
Samples without dna

Groups and cohorts

  • patients with noninfectious uveitis

    including pediatric connective tissue disorders, granulomatosis, idiopathic juvenile arthritis without uveitis, pediatric vasculitis, and chronic inflammatory bowel diseases. These conditions were selected because of their inflammatory and/or autoimmune nature, making it possible to determine whether fecal peptidoglycan signatures

  • patients with another inflammatory disease

    without uveitis (connective tissue disease, granulomatosis, juvenile idiopathic arthritis, pediatric vasculitis, chronic inflammatory bowel disease)

  • healthy children living in the same household as those who are sick

    Siblings of patients or children of hospital staff, who may be included as healthy control groups

06

What researchers measure

Primary outcomes

  1. fecal peptidoglycans

    the composition and relative abundance of fecal PG fragments in children with uveitis compared to healthy children.

    Time frame: Day 1

Secondary outcomes

  1. Gut Microbiome

    * Correlations between the peptidoglycans and the gut microbiota, as determined by sequencing. * Analysis of fecal microRNAs (miRNAs) and their correlations with the peptidoglycans and the microbiota. * Analysis of associations between the peptidoglycans and the microbiota, miRNAs, and clinical parameters: uveitis activity, ophthalmic complications, and patient metadata. * Comparison with the additional control group (non-ocular inflammatory diseases) to identify signatures specific to uveitis versus those associated with a systemic inflammatory condition.

    Time frame: Day 1

07

Study locations

1 site
  • Hôpital Robert Debré - APHP
    Paris, 75019, France
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Nov 2026; primary completion for Nov 2028, 24 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 13, 2026
First posted
Oct 21, 2026
StartEst.
Nov 2026
Primary completionEst.
Nov 2028
CompletionEst.
Dec 2028
Last update
Oct 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07885501
Responsible party
Sponsor
First posted
Oct 21, 2026
Start date
Nov 2026 (estimated)
Primary completion
Nov 2028 (estimated)
Completion
Dec 2028 (estimated)
Last update
Oct 21, 2026

Study contacts

Ulrich Phd Meinzer, PhD
Contact
ulrich.meinzer@aphp.fr
+33 140 03 25 99
Ulrich Meinzer, PhD
study chair · APHP

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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