Lupus Patients' quality of life under the microscope in new study
NCT ID NCT01904812
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 356 adults with lupus over time to see how the disease impacts their quality of life. Participants filled out questionnaires about their symptoms, fatigue, mood, and daily activities. The goal was to better understand what factors affect well-being in lupus, without testing any new treatments.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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356 people
The number who actually took part.
- Started
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Dec 2011
- Finished
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May 2015
- 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.
- Ages
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18 to 75 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * \- Patients meeting ACR 1997 classification criteria for systemic lupus erythematosus. * Patients able to understand written and spoken French. * Patients aged from 18 to 75 years * Patients who have received written and oral information about the research. Exclusion Criteria: * \- Patients aged less than 18 years * Patients aged more than 75 years * Severe mental retardation Any impairment of abilities to understand that make self-evaluation impossible
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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.
Contacts and locations
Locations
-
CHU de Dijon
Dijon, 21079, France
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Other studies related to the condition(s) this trial covers.
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