ClinicalTrials.gg
Not yet recruitingNCT07831291MARIOBEUpdated Sep 21, 2026

Childhood Obesity Risk Markers (MARIOBE)

An interventional study of early transcriptomic markers in Obesity & Overweight, sponsored by University Hospital, Clermont-Ferrand. Not yet recruiting at 1 site in France. Open to participants aged 1 Day to 4 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-21.

Sponsored by University Hospital, Clermont-Ferrand · Not applicable, Interventional, and Screening

Phase
Not applicable
Study type
Interventional
Enrollment
400
Allocation
Not applicable
Ages
1 Day to 4 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 44 studies in Obesity by University Hospital, Clermont-Ferrand — 6 open to participants now, 6 under way, none of them phase 3. Obesity · University Hospital, Clermont-Ferrand.

Planned enrollment
4th of 37
400 · median 40
Started
2026
with 2 others
No phase
34 of 44
6 open now
Registered
44th of 44
by date

Among the 44 studies in Obesity by University Hospital, Clermont-Ferrand, this one is the 4th largest by planned enrollment of the 37 interventional ones that give a count, is one of 3 that started in 2026, is one of 34 with no phase, and was the 44th registered.

Obesity

11,522 studies on the registry are indexed under Obesity; 2,033 are open to participants now.

Browse Obesity studies →

Open to participants now

6 of the 44 studies in Obesity by University Hospital, Clermont-Ferrand are open now, in 1 country. Recruiting first, the newest first:

By country, each count listing its studies:

All 6 open studies →

Where they have run

Who these studies take

Of the 1,336 Obesity studies recruiting now, 377 (28%) set no upper age limit and 856 (64%) stop at 75 or younger; 168 take children under 18; 491 take healthy volunteers.

This study: 1 Day to 4 Years · all sexes · healthy volunteers too.

The full table on the hub →

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02

Study summary

Metabolic diseases, including childhood obesity, represent a major public health challenge. Studies in mice have identified transcriptomic markers in adipose tissue capable of predicting a predisposition to obesity prior to any weight gain. The MARIOBE project aims to translate this approach to young children (≤ 4 years old) in order to identify individual vulnerability to obesity at an early stage.

03

Conditions studied

  • Obesity & Overweight

Keywords

  • obesity
  • transcriptomic
  • overweight
  • children
04

Who can participate

Ages eligible
1 Day to 4 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

  • Child scheduled for surgery allowing for the harvesting of adipose tissue.

Exclusion criteria

Exclusion Criteria:

  • Child whose holders of parental authority are protected by law
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
400 participants (estimated)

Study arms

  • Experimental
    early transcriptomic markers

    Other: early transcriptomic markers

Interventions

  • Otherearly transcriptomic markers

    during a scheduled surgery before the age of 4 years, collection of a blood sample (2.5 mL in a PAXgene tube) and two adipose tissue fragments, each measuring 5 mm x 5 mm x 5 mm. tracking of weight and height curves from birth to age 6

06

What researchers measure

Primary outcomes

  1. transcriptomic markers in children under 4 years of age that predict a predisposition to being overweight at age 6 (BMI > IOTF25).

    Ranking of the discriminative capacity of adipocyte and blood transcripts before 4 years of age to predict the development of overweight (BMI \> IOTF25) at age 6, using Partial Least Squares Discriminant Analysis (PLS-DA).

    Time frame: perioperative

Secondary outcomes

  1. analyze weight trajectories

    Selection and validation of transcriptomic markers for the development of a predictive score for the risk of overweight and obesity in children

    Time frame: at age 6 years

  2. molecular and epigenetic mechanisms associated with the identified transcriptomic signatures.

    methylation profiles

    Time frame: at the time of blood ans adipose tissu sampling

  3. comparison of transcriptomic expression levels between blood and adipose tissue

    percentage of common markers sampled from blood and adipose tissue

    Time frame: perioperative

  4. develop a quantitative test based on digital PCR to define individual expression thresholds predictive of risk

    Performance of the digital PCR test evaluated by the ability to discriminate weight trajectories (AUC of ROC curves).

    Time frame: at age 6 years

07

Study locations

1 site
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Sep 2036, 120 months later.

Of 3,680 non-industry interventional studies with no phase under Obesity, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 43. This study's planned 120 months is above that.

Counting every sponsor, half of 3,843 studies reached it within 22 months; a quarter within 10 and three quarters within 42.

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

Registered
Sep 8, 2026
First posted
Sep 21, 2026
StartEst.
Sep 2026
Primary completionEst.
Sep 2036
CompletionEst.
Sep 2036
Last update
Sep 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.
No changes since tracking began. The registry record was last updated on Sep 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07831291
Responsible party
Sponsor
First posted
Sep 21, 2026
Start date
Sep 2026 (estimated)
Primary completion
Sep 2036 (estimated)
Completion
Sep 2036 (estimated)
Last update
Sep 21, 2026

Study contacts

Lise Laclautre
Contact
promo_interne_drci@chu-clermontferrand.fr
+334754963
Etienne Merlin
principal investigator · University Hospital, Clermont-Ferrand

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 Jul 2026. You cannot join it, but the record below documents what was studied.

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