New registry tracks Morphea's mysterious behavior over time
NCT ID NCT01808937
First seen May 20, 2026 · Last updated May 20, 2026
Summary
This study creates a registry for people with morphea (localized scleroderma) to better understand how the disease changes over time, what other health issues may occur (like arthritis), and whether it is autoimmune. Researchers will follow up to 500 children and adults for years, using skin exams and quality-of-life surveys. No new treatments are being tested; the goal is simply to learn more about the condition.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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UT Southwestern Medical Center - Department of Dermatology
RECRUITINGDallas, Texas, 75390-9069, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
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