Scleroderma biomarker study pulled before start
NCT ID NCT04986514
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study planned to collect extra blood and urine samples from scleroderma patients during their regular check-ups to find biological markers that could predict if their disease would get worse over the next 10 years. The goal was to improve treatment decisions and identify the right patients for future clinical trials. However, the study was withdrawn before any participants were enrolled, so no results are available.
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Study facts
What this study's own registry entry says, in plain language.
- Expected to start
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Apr 2023
An estimate. Start dates often move.
- Expected to finish
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Apr 2043
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patient followed for SSc in the internal medicine or cardiology department of the Lille University Hospital
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient followed for SSc in the internal medicine or cardiology department of the Lille University Hospital * Fulfilling the ACR/EULAR and/or VEDOSS criteria for SSc * Being insured by the French social security system * Having the ability to understand the requirements of the study and provide informed consent Exclusion Criteria: * Administrative reasons: unable to receive informed information, lack of social security coverage * Pregnant or lactating women * Persons deprived of liberty * Minors or protected adults * Persons who have refused or are unable to give informed consent * Persons in emergency situations
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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Other studies related to the condition(s) this trial covers.
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