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

  • Hôpital Cochin

    Paris, 75679, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.