Study of Genetic Test for Renal Pseudohypoaldosteronism Type1

Study of Genetic Test for Renal Pseudohypoaldosteronism Type1 - Genetic Test for Renal Pseudohypoaldosteronism Type1

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000023364

Enrollment

Registered

2016-07-27

Start date

2016-08-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal pseudohypoaldosteronism type1

Interventions

Detect mutations in the gene of renal pseudohypoaldosteronism type1 known as NR3C2 with direct sequence

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who suffers dehydration or hyperkalemia of uncertain cause and are suspected of having renal pseudohypoaldosteronism type1

Exclusion criteria

Exclusion criteria: In case they have other known disease causing gene mutations

Design outcomes

Primary

Measure	Time frame
To affirm the strictness of genetic test for renal pseudohypoaldosteronism type1	—

Countries

Japan

Contacts

Public ContactNaoaki Mikami

Tokyo Metropolitan Children's Medical Center Department of Nephrology

naoaki_mikami@tmhp.jp042-300-5111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026