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Nephrogenic diabetes insipidus

MONDO:0016383

Nephrogenic diabetes insipidus (NDI) is characterized by polyuria with polydipsia, recurrent bouts of fever, constipation, and acute hypernatremic dehydration after birth that may cause neurological sequelae. Polyuria may exceed 10 liters in children.

Also known as: ADH resistant diabetes insipidus, diabetes insipidus nephrogenic, diabetes insipidus nephrogenic X-linked, diabetes insipidus nephrogenic type 1

35 clinical trials for this condition and its sub-types.

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Sub-types

Diabetes insipidus, nephrogenic, X-linked (1) Diabetes insipidus, nephrogenic, autosomal (0)

Broader categories

Disease (680) Kidney disorder (214) Hereditary disease (176) Impaired renal function disease (108) Urinary system disorder (66) Diabetes insipidus (33) Human disease (14) Disease of genetic or genomic mechanism (2) Inherited kidney disorder (1) Renal tubule disorder (1)

Trials to join now! 10 Not yet recruiting 6 Not yet finished but already full! 1 Completed 18

Withdrawn study sought safer biopsies for Bleeding-Prone patients

Knowledge-focused Terminated

This study planned to test a technique called radiofrequency track cautery during liver, kidney, or spleen biopsies in patients at high risk for bleeding. The idea was to use a small heated probe to seal the biopsy track and reduce bleeding. However, the study was withdrawn befor…

Phase: NA • Sponsor: Brigham and Women's Hospital • Aim: Knowledge-focused

Last updated Jun 27, 2026 07:56 UTC