Actively Recruiting

All Genders
ID03465150

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

Led by Nantes University Hospital · Updated on 2026-04-13

200

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying acne, a common skin condition with significant psychosocial effects, through a unique cohort at Nantes University Hospital. This observational study aims to identify factors predicting treatment response, assess the severity and impact on quality of life, and understand the costs associated with acne. The team will also collect bacteriological samples to further investigate acne's causes and influences. Patients visiting the specialized acne consultation at Nantes University Hospital for the first time and meeting eligibility criteria will join the cohort. Follow-up visits are scheduled individually based on medical need, usually between one and four months apart. The study includes gathering blood samples for hormonal checks and bacteriological samples to detect Propionibacterium acnes. Participants will have their acne stage measured and quality of life assessed over two years. Researchers will monitor psychological impact, treatment courses, and related expenses. The cohort will gather detailed data through clinical evaluations, questionnaires, and biological samples, helping to improve understanding and management of acne with ongoing observation throughout the study period.

CONDITIONS

Brief Title

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

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient with acne
  • Patient or legal guardian agrees to participate
  • Covered by appropriate health insurance
Not Eligible

You will not qualify if you...

  • Other facial skin conditions besides acne
  • Refusal to participate by patient or guardian
  • Adults under legal protection such as guardianship or trusteeship

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 2 years

Participants who attend specialized acne consultations are observed over time with follow-up visits based on their medical needs.

Visits every 1 to 4 months depending on medical needs

Trial Site Locations

Total: 1 location

1

CHU de Nantes

Nantes, France, 44000

Actively Recruiting

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Research Team

B

Brigitte DRENO

A

Amir khammari

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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