Pemphigus study digs into hidden emotional struggles

NCT ID NCT02237313

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at 48 adults with pemphigus, a rare blistering skin disease, to understand what makes them feel vulnerable during their illness. Researchers used interviews and questionnaires to explore factors like misdiagnosis, differences in how patients and doctors see disease severity, and how patients use health information. The goal was to identify patterns that could help improve support for patients.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to
If successful, this could help doctors identify which pemphigus patients need extra psychological support, leading to better overall care.
What could go wrong
This is a small, completed observational study (48 people) that only identifies factors—it does not test a treatment, so it won't directly change outcomes.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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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

  • CH du Mans

    Le Mans, 72037, France

  • CHRU de Lille Hôpital Claude Huriez

    Lille, 59037, France

  • CHU de Clermont-Ferrand Hôpital d'Estaing

    Clermont-Ferrand, 63003, France

  • Centre hospitalier de Cornouaille

    Quimper, 29107, France

  • Hôpital Avicenne

    Bobigny, 93000, France

  • Hôpital Haut-Lévêque

    Pessac, 33604, France

  • Hôpital La Timone, Assistance publique hôpitaux de Marseille-Aix

    Marseille, France

  • Hôpital Robert Debré, chu de Reims

    Reims, 51 092, France

  • University Hospital of Rouen

    Rouen, 76031, France

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