A Multi-center, Prospective Evaluation of Infants and Children With Congenital Ichthyosis

Stopped early

Conditions studied: Ichthyosis

In brief

This project will follow babies with ichthyosis over time in order to better understand the natural course of ichthyosis in infants and children and to examine how specific genetic mutations affect clinical characteristics.

Key facts

Study ID

NCT02655861

Run by

Yale University

People needed

21

Starts

2015-06-01

Expected to finish

2019-06-05

Last updated by the study team

2020-07-07

Who can join

Age: any, up to 3. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• One parent must be able to understand and sign an informed consent document.
• Newborns who present at or within 2 months of birth with a clinical diagnosis of ichthyosis.
• Families must consent to providing DNA for genetic analysis
• Families must agree to the intake evaluation followed by 10 follow-up evaluations, which will occur at ages 1, 2, 3, 6, 9, 12, 18, 24, and 36 months.

You may not qualify if…

• Subjects with non-English speaking parents
• Patients with a family history of ichthyosis vulgaris
• Patients with X-linked ichthyosis

Where it is running

• Yale School of Medicine — New Haven, Connecticut, United States

Full record on ClinicalTrials.gov

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