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Study of Novel Types of Familial Diabetes Insipidus
This study is ongoing, but not recruiting participants.
Study NCT00004364   Information provided by Office of Rare Diseases (ORD)
First Received: October 18, 1999   Last Updated: February 21, 2006   History of Changes

October 18, 1999
February 21, 2006
December 1995
 
 
 
Complete list of historical versions of study NCT00004364 on ClinicalTrials.gov Archive Site
 
 
 
Study of Novel Types of Familial Diabetes Insipidus
 

OBJECTIVES:

I. Define the phenotype and genotype of previously unrecognized types of familial diabetes insipidus (FDI) in kindreds with atypical or novel forms of FDI.

PROTOCOL OUTLINE: Participants undergo a series of tests to determine the presence, absence, cause, natural history, clinical status, and mode of inheritance of their type of diabetes insipidus (DI). The studies include measurements of basal fluid intake and urine output, plasma vasopressin during standard fluid deprivation or waterload/saline infusion tests, and changes in water balance during a therapeutic trial of DDAVP. If clinically indicated, echocardiograms and assays of plasma catecholes and renin are also completed.

Linkage analysis is performed for all participants; kindreds with the Marfan-like syndrome are also studied for the fibrillin-1 genotype.

Participants determined to have DI are treated with desmopressin for 2 days.

 
Observational
Screening
Diabetes Insipidus
Drug: desmopressin
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
5
 
 
  • Familial diabetes insipidus (DI) in atypical or novel form, e.g.: Dipsogenic DI Neurohypophyseal DI
  • Affected and unaffected members of kindreds eligible
Both
6 Months to 70 Years
No
Contact information is only displayed when the study is recruiting subjects
 
 
NCT00004364
 
199/11939, NU-570
National Center for Research Resources (NCRR)
Northwestern University
Study Chair: Gary L. Robertson Northwestern University
Office of Rare Diseases (ORD)
February 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP