Rare disease CACP syndrome under the microscope: new study aims to unlock its secrets
NCT ID NCT07468461
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study is gathering information from 15 people with CACP syndrome, a rare genetic condition that causes joint problems and sometimes heart issues. Researchers want to better understand how the disease develops and changes over time. The goal is to improve diagnosis and care for patients with this condition.
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 study could lead to a better understanding of CACP syndrome, improving diagnosis and management for patients.
- What could go wrong
- This is an observational study with only 15 participants, so findings may not apply to all patients. No new treatment is being tested.
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
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ASST Fatebenefratelli
NOT_YET_RECRUITINGMilan, Italy
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Ankara Pediatrik Romatoloji Bilim Dalý Hacettepe Üniversitesi
NOT_YET_RECRUITINGAnkara, 06105, Turkey (Türkiye)
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Azienda Ospedaliera di Padova
NOT_YET_RECRUITINGPadova, Italy
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Centro di Reumatologia Pediatrica
NOT_YET_RECRUITINGUdine, Italy
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Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
RECRUITINGMilan, Italy
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Hiospedal Sant Joan de Déu
NOT_YET_RECRUITINGBarcelona, 208950, Spain
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IRCCS Istituto Giannina Gaslini,
RECRUITINGGenova, Italy
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Ospedale Pediatrico Giovanni XXIII
NOT_YET_RECRUITINGBari, Italy
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Rheumatology Unit, Meyer Children's Hospital
RECRUITINGFlorence, Italy
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Santa Maria Goretti Hospital
NOT_YET_RECRUITINGRoma, Italy
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