Bartter disease type 4B
MONDO:0000909A Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes.
Also known as: BARTS4B, Bartter disease type 4B, Bartter syndrome, type 4B, Bartter syndrome, infantile, with sensorineural deafness, Bartter syndrome, type 4B, neonatal, with sensorineural deafness
11 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
ER study aims to uncover hidden kidney problems in kids
Knowledge-focused Not yet recruitingThis study will observe 50 children (ages 1 month to 18 years) who come to the emergency room with kidney-related symptoms like swelling, blood in urine, or high blood pressure. Researchers want to learn which kidney diseases are most common and how children respond to initial tr…
Sponsor: Sohag University • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:23 UTC
-
30,000 blood samples could revolutionize rapid disease testing
Knowledge-focused Not yet recruitingThis study will collect blood samples from 30,000 adults in the UK with various health conditions, including blood clots, infections, heart disease, diabetes, and more. The samples will be used to develop and fine-tune new diagnostic tests for the cobas® lumira device, which allo…
Sponsor: LumiraDx UK Limited • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:00 UTC