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RecruitingNCT03465150COPACNEUpdated Apr 13, 2026

Creation of a Monocentric Cohort of Patients Treated for Acne at the Nantes University Hospital

An observational study in Acne, sponsored by Nantes University Hospital. Recruiting at 1 site in France. Per ClinicalTrials.gov, last updated 2026-04-13.

Sponsored by Nantes University Hospital · Observational

From the registry’s dates

  • Started Sep 2018; still recruiting 8 years 1 month later.

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Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
200
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 24 studies in Acne Vulgaris with a site in France — 3 open to participants now, 4 under way, 1 of them phase 3. Acne Vulgaris · France.

Started
2018
with 3 others
Observational
6 of 24
1 open now
Registered
8th of 24
by date
Lead sponsor
2 of 24
Nantes University Hospital

Among the 24 studies in Acne Vulgaris with a site in France, this one is one of 4 that started in 2018, is one of 6 observational ones, and was the 8th registered.

Acne Vulgaris

791 studies on the registry are indexed under Acne Vulgaris; 94 are open to participants now.

Browse Acne Vulgaris studies →

Open to participants now

3 of the 24 studies in Acne Vulgaris with a site in France are open now. Recruiting first, the newest first:

All 3 open studies →

A study can be open while its sites in France have not opened yet or have stopped. Only those recruiting at a site in France →

Who these studies take

Of the 47 Acne Vulgaris studies recruiting now, 17 (36%) set no upper age limit and 29 (62%) stop at 75 or younger; 21 take children under 18; 17 take healthy volunteers.

This study: all sexes · no healthy volunteers.

The full table on the hub →

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 24 studies in Acne Vulgaris with a site in France, or all of them as a file.
02

Study summary

With 24 million results associated with Google's searchon keywords "severe acne", Pr Dreno's team understand better thatthis disease, which affects many French people, is a real concern of Public Health and not a "forced evil" of the adolescent period, which will eventually resolve itself. Acne does not affect the vital prognosis, but its psychosocial impact is major and should not be underestimated. Paradoxically, despite the high prevalence of acne, few quality epidemiological studies have been published. Physicians are often helpless when faced with patients' questions. They often need a lot of explanations, especially on the factors aggravating this dermatosis, which greatly affects their quality of life.

This cohort, the first of its kind in France, will determine the predictive factors of therapeutic response, endogenous and environmental factors impacting on the severity of acne assess the quality of life and psychological impact of acne patients, determine the patient's course of care and the associated costs. Pr Dreno's team will also build up a bio collection (bacteriological samples).

Read the detailed description

All patients going for the first time in specialized consultation "acne" at Nantes University Hospital , and who meet the inclusion criteria will be included in the COPACNE cohort. Inclusion will take place at the first consultation, after information and agreement of the patient and, if applicable, his or her legal representatives. The frequency of each patient's follow-up visits will be determined on a case-by-case basis according to the patient's medical needs (generally, the interval between 2 visits is between 1 and 4 months).

03

Conditions studied

  • Acne

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Keywords

  • Acne
  • Cohort
  • prospective
  • risk factors
04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients going for the first time in specialized consultation "acne"

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

  • Patient with acne
  • Patient (or parents/guardians for minors) who are not opposed to participating in the cohort.
  • Subjects affiliated to an appropriate health insurance

Exclusion criteria

Exclusion Criteria:

  • Dermatosis of the face other than acne
  • Refusal to participate by the minor or parent/guardian
  • Adults under a legal protection regime (guardianship, trusteeship, judicial safeguard)
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
200 participants (estimated)
Target follow-up
2 Years
Patient registry
Yes

Interventions

  • Otheracne

    Patient with acne

    Also known as: acne vulgaris

06

What researchers measure

Primary outcomes

  1. Measure of Acne stage

    composite criteria. the scale is GEA for Global Evaluation Acne Scale with 0 no acne to 5 severe acne

    Time frame: 2 years

Secondary outcomes

  1. assessing patients' quality of life

    composite criteria. CADI score is calculated by summing the score of each question resulting in a possible maximum of 15 and a minimum of 0. The higher the score, the more the quality of life is impaired.

    Time frame: 2 years

  2. cost of acne illness

    reimbursement data relating to hospitalizations and care in town recorded by the Health Insurance in the SNIIRAM database.

    Time frame: 2 years

  3. Bacteriological sample to find Propionibacterium acnes, Hormonal check-up on blood sample

    Correlation between bacterial and blood samples and the efficacity of the treatment

    Time frame: 2 years

07

Study locations

1 of 1 sites recruiting
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

Started Sep 2018 (actual). Primary completion is estimated for Feb 2033, 173 months after the start.

Of 37 observational studies under Acne Vulgaris, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 13. This study's planned 173 months is above that.

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

Registered
Feb 5, 2018
First posted
Mar 14, 2018
StartActual
Sep 23, 2018
Primary completionEst.
Feb 28, 2033
CompletionEst.
Dec 28, 2033
Last update
Apr 13, 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 Apr 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03465150
Responsible party
Sponsor
First posted
Mar 14, 2018
Start date
Sep 23, 2018
Primary completion
Feb 28, 2033 (estimated)
Completion
Dec 28, 2033 (estimated)
Last update
Apr 13, 2026

Study contacts

Brigitte DRENO
Contact
brigitte.dreno@wanadoo.fr
0240083137
Amir khammari
Contact
amir.khammari@chu-nantes.fr
Brigitte DRENO, PU-PH
principal investigator · Nantes University Hospital

Oversight

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

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