Actively Recruiting
Registry of Psoriasis Health Outcomes: A Real-world Observational Study of Deucravacitinib Effectiveness in Adults With Moderate-to-Severe Plaque Psoriasis in France
Led by Bristol-Myers Squibb · Updated on 2026-05-18
350
Participants Needed
48
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the real-world effectiveness of deucravacitinib in adults diagnosed with moderate-to-severe plaque psoriasis. This observational study aims to understand how this treatment works outside of controlled clinical trials, focusing on health outcomes important to patients and doctors. It is sponsored by Bristol-Myers Squibb and conducted in France. Participants in this study have started treatment with deucravacitinib as prescribed by their doctors. The study observes these patients over time without altering their treatment plans. There are no placebo or comparison groups since this is an observational study that follows patients initiating deucravacitinib treatment. During the study, doctors will assess skin condition using the Physician's Global Assessment and measure quality of life with the Dermatology Life Quality Index at baseline and several points up to 24 months. Patients will also report symptoms like itch, skin pain, and fatigue using visual scales. Researchers will track how long patients remain on treatment and reasons for stopping. The study involves regular follow-ups at months 1, 4, 12, 18 (optional), and 24 to gather this information.
CONDITIONS
Brief Title
A Real-world Study to Evaluate the Effectiveness of Deucravacitinib in Adults With Plaque Psoriasis in France (RePhlect)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Physician-reported diagnosis of moderate to severe plaque psoriasis
- Newly starting deucravacitinib treatment
- Agree to participate in the study
You will not qualify if you...
- Currently participating in or planning to participate in an interventional clinical trial
- Previous treatment with deucravacitinib, including in a blinded, randomized trial
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 24 months
Participants receive deucravacitinib as prescribed by their treating clinician and are monitored to evaluate its effectiveness.
Visits at baseline and months 1, 4, 12, 18 (optional), and 24
Trial Site Locations
Total: 48 locations
1
Chu Amiens Picardie - Site Sud
Amiens, France, 80054
Actively Recruiting
2
Cabinet Médical Elisabeth Lion
Angers, France, 49100
Actively Recruiting
3
Ch Victor Dupouy
Argenteuil, France, 95107
Actively Recruiting
4
Local Institution - 089
Argenteuil, France, 95107
Completed
5
CH ARRAS
Arras, France, 62000
Actively Recruiting
6
Cabinet Dermatologie
Bordeaux, France, 33200
Actively Recruiting
7
Cabinet Dermatologie
Bordeaux, France, 33200
Actively Recruiting
8
Centre Hospitalier William Morey - Hématologie
Chalon-sur-Saône, France, 71100
Actively Recruiting
9
Local Institution - 053
Clermont-Ferrand, France, 63000
Completed
10
CHU Dijon
Dijon, France, 21000
Actively Recruiting
11
Local Institution - 077
Dijon, France, 21000
Not Yet Recruiting
12
CHU Grenoble Alps, Service de Dermatologie
La Tronche, France, 38700
Actively Recruiting
13
Local Institution - 014
Le Mans, France, 72037
Not Yet Recruiting
14
CH Emile Roux
Le Puy-en-Velay, France, 43000
Actively Recruiting
15
Centre Hospitalier Lens
Lens, France, 62307
Actively Recruiting
16
Centre de santé Filieris
Marcq-en-Barœul, France, 59700
Actively Recruiting
17
Hopital Saint Eloi
Montpellier, France, 34295
Actively Recruiting
18
Tagast 41
Nice, France, 06000
Actively Recruiting
19
Ch Georges Renon
Niort, France, 79021
Actively Recruiting
20
Ch Georges Renon
Niort, France, 79021
Actively Recruiting
21
Hopital Caremeau
Nîmes, France, 30900
Actively Recruiting
22
Cabinet de dermatologie
Paris, France, 75012
Actively Recruiting
23
Local Institution - 086
Paris, France, 75012
Completed
24
Hôpital Privé Francheville
Périgueux, France, 24000
Actively Recruiting
25
Centre Hospitalier de Roubaix
Roubaix, France, 59056
Actively Recruiting
26
Centre Hospitalier de Roubaix
Roubaix, France, 59056
Actively Recruiting
27
Local Institution - 031
Rouen, France, 76031
Completed
28
Local Institution - 065
Saint-Germain-en-Laye, France, 78100
Not Yet Recruiting
29
Hia Begin
Saint-Mandé, France, 94163
Actively Recruiting
30
Centre Dermatologique
Saint-Maur-des-Fossés, France, 94100
Actively Recruiting
31
Hia Sainte Anne
Toulon, France, 83800
Actively Recruiting
32
Hia Sainte Anne
Toulon, France, 83800
Actively Recruiting
33
Hopital Larrey
Toulouse, France, 31059
Actively Recruiting
34
Hopital Larrey
Toulouse, France, 31059
Actively Recruiting
35
Hopital Larrey
Toulouse, France, 31059
Actively Recruiting
36
Hopitaux de Brabois
Vandœuvre-lès-Nancy, France, 54511
Actively Recruiting
37
Hopitaux de Brabois
Vandœuvre-lès-Nancy, France, 54511
Actively Recruiting
38
Médipôle Hôpital Mutualiste
Villeurbanne, France, 69100
Actively Recruiting
39
Médipôle Hôpital Mutualiste
Villeurbanne, France, 69100
Actively Recruiting
40
Cabinet Medical
La Chaux-de-Fonds, Switzerland, 2300
Actively Recruiting
41
Cabinet Medical
La Chaux-de-Fonds, Switzerland, 2300
Actively Recruiting
42
Cabinet Medical
La Chaux-de-Fonds, Switzerland, 2300
Actively Recruiting
43
Cabinet Medical
La Chaux-de-Fonds, Switzerland, 2300
Actively Recruiting
44
Cabinet Medical
La Chaux-de-Fonds, Switzerland, 2300
Actively Recruiting
45
Cabinet Medical
La Chaux-de-Fonds, Switzerland, 2300
Actively Recruiting
46
Cabinet Medical
La Chaux-de-Fonds, Switzerland, 2300
Actively Recruiting
47
Local Institution - 056
La Chaux-de-Fonds, Switzerland, 2300
Completed
48
Local Institution - 059
La Chaux-de-Fonds, Switzerland, 2300
Completed
Research Team
B
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
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First line of the email MUST contain NCT # and Site #.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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