Cohort of patients treated for acne at Nantes University Hospital
Creation of a Monocentric Cohort of Patients Treated for Acne at the Nantes University Hospital: the COPACNE Cohort.
This study is looking at first-time acne patients at Nantes University Hospital to see how different factors affect their acne and their quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Sex | All |
| Sponsor | Nantes University Hospital Academic / other |
| Locations | 1 site (Nantes) |
| Trial ID | NCT03465150 on ClinicalTrials.gov |
What this trial studies
This observational cohort study aims to gather data from patients visiting the specialized acne consultation at Nantes University Hospital for the first time. It will assess various factors influencing the severity of acne, including both endogenous and environmental elements, while also evaluating the quality of life and psychological impact on patients. The study will include patients who consent to participate and will follow them over time to determine therapeutic responses and other relevant outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are patients with acne who are visiting the specialized consultation for the first time and agree to participate.
Not a fit: Patients with facial dermatosis other than acne or those who refuse to participate will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the factors affecting acne treatment and improve management strategies for patients.
How similar studies have performed: While there have been few quality epidemiological studies on acne, this cohort represents a novel approach in France to better understand the condition.
Eligibility criteria
Show full inclusion / exclusion criteria
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: * 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)
Where this trial is running
Nantes
- CHU de Nantes — Nantes, France (Recruiting)
Study contacts
- Principal investigator: Brigitte DRENO, PU-PH — Nantes University Hospital
- Study coordinator: Brigitte DRENO
- Email: brigitte.dreno@wanadoo.fr
- Phone: 0240083137
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.