International Clinical Trial: Clinical and genetic analysis of Liddle syndrome caused by a novel de novo nonsense mutation in the SCNN1B gene

Geneva, Aug. 6 -- International Clinical Trials Registry received information related to the study (ChiCTR2600128629) titled 'Clinical and genetic analysis of Liddle syndrome caused by a novel de novo nonsense mutation in the SCNN1B gene' on July 23.

Study Type: Observational study

Study Design: Case study

Primary Sponsor: Fuzhou University Affiliated Provincial Hospital

Condition: Liddle syndrome (early-onset hypertension, hypokalemia, suppressed renin, low aldosterone)

Recruitment Status: Not Recruiting

Phase: N/A

Date of First Enrollment: 2026-07-23

Target Sample Size: Proband group:4;

Countries of Recruitment: China

To know more, visit https://www.chictr.org.cn/showproj.html?proj=334005

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