Researchers track rare hormone disorder in 133 patients
NCT ID NCT00668291
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 133 people with PPNAD (a rare adrenal gland disorder) or Carney Complex (a related genetic condition) for three years. The goal was to better understand the symptoms and genetic causes of these diseases, not to test a new treatment. Participants had yearly check-ups including clinical exams, genetic testing, and imaging.
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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
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Hôpital Cochin
Paris, 75679, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.