Study Description
Screening
Study Centers
Contact/Consent
Eczema/Dermatitis
Also called atopic eczema, this is a chronic, hereditary, condition often triggered by environmental factors. The skin itches intensely and is dry and inflamed, with episodes of redness, weeping, crusting, cracking, and scaling. Atopic dermatitis most often affects infants and young children, but it can continue into adulthood or even first occur later in life. The condition fluctuates, with exacerbations or flares. The disease is associated with other so-called atopic disorders, such as hay fever and asthma.
Novartis is seeking people to participate in a clinical trial(s) testing the safety
and effectiveness of Novartis products. Novartis recommends that you consult your
doctor before participating in a clinical trial.
How to use this system:
The purpose of this system is to help connect interested study participants with clinical
research centers. The following is a brief outline explaining the main steps involved in
using this system. Please note that every step in this process is optional.
1. Select a clinical trial that you feel best suits your (or the participant's)
health condition.
2. Answer the screening questions to see if you (or the participant) meet
the preliminary qualifications for
the study. The answers to these questions
are not retained by this system.
3. Select a study center to contact for additional information about the
clinical trial.
4. Set up an account and agree to the terms of use for this system.
5. Submit your information to the study center you selected.
6. The study center may contact you and may ask more questions about your
(or the participant's) eligibility
for the study. The study center may invite you
(and the participant if applicable) to travel to the study center
for additional screening tests. Novartis cannot guarantee that you
will be contacted by the study center.
7. If you are eligible to participate in the study, then you will be required
to sign an
informed consent before enrolling in the study. An informed consent
is provided to you to help you understand the clinical trial, the nature of
the medical treatment (if any),
procedures and known risks involved, before you agree to participate in the study.
For more information about clinical trial participation, click here. Also, for additional information
about how Novartis helps to protect the privacy of the personal information that you provide to us, please
see the Novartis Privacy Policy.
Please review the details of the clinical trial(s) listed below and click on the one that you feel best suits
your (or the participant's) condition.
Pediatric Eczema Elective Registry (PEER Program)
Novartis Pharmaceuticals Corporation is sponsoring a Pediatric Eczema Elective Registry (PEER) to monitor the long-term safety of topical calcineurin inhibitors. This scientific observational registry is designed to collect information from the parents of approximately 5000 children across the USA between the ages of 2 years and 17 years (at enrollment) who have used and may continue to use ElidelĀ® for the treatment of eczema. For more information on this program, please visit www.childrenseczemaregistry.com or call 1-877-711-7337.
Trial phase: Phase 4
Participation Duration: Up to 10 years from the time of enrollment.
Protocol Number: CASM981CUS2311
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