Scleroderma patients needed for landmark registry study

NCT ID NCT01656447

First seen Jan 05, 2026 · Last updated May 07, 2026 · Updated 20 times

Summary

This study is creating a registry of 300 adults with scleroderma to collect medical information and samples over time. The goal is to learn more about the disease's features, genetics, and biology, which could lead to future treatments. Participants will provide skin scores and complete health questionnaires.

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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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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Hospital for Special Surgery

    RECRUITING

    New York, New York, 10021, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

    Contact

Conditions

Explore the condition pages connected to this study.