150 patients studied to map rare kidney Disease's Long-Term effects
NCT ID NCT01022957
First seen Nov 20, 2025 · Last updated May 23, 2026 · Updated 24 times
Summary
This study followed 150 people with nephronophthisis, a rare genetic kidney disease, to see how it damages the kidneys and other organs over many years. Participants had confirmed mutations in one of several genes (NPHP1 through NPHP8) and were at least 7 years old. The goal was to better predict and manage complications, not to test a new treatment.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for NEPHRONOPHTHISIS are added.
Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Locations
-
Hopital Necker
Paris, 75015, France
Conditions
Explore the condition pages connected to this study.