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Search/NCT00001552
NCT00001552N/ACompleted

Characteristics of Idiopathic Familial Voice Disorders

National Institute of Neurological Disorders and Stroke (NINDS)·observational·Posted Nov 4, 1999·Updated Jul 2, 2017

In Brief

An observational study for Laryngeal Disease and 2 related conditions. Completed, across 4 sites in 2 countries.

Detailed Summary

The purpose the study is to determine the genetic causes of specific voice disorders that run in families. Researchers are particularly interested in two conditions; 1. Spasmodic dysphonia 2. Vocal fold paralysis Familial vocal fold paralysis can be a life-threatening disorder that can cause difficulty with vocal fold movement for breathing and voice and sometimes for swallowing. Studies are ongoing at the NIH to better understand the pathophysiology and to relate it to the genetic pattern of inheritance. Families are being recruited to participate in these studies and are being provided with further information on the disorder and genetic counseling if desired. Physician referral is requested for affected members of families with vocal fold paralysis of an unknown cause occurring over at least 2 generations. All travel, lodging, examination and counseling costs are covered for both affected and unaffected members of a family. Examinations include: voice, laryngeal, neurological, electrodiagnostic testing, genetic counseling, and radiological studies....

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited Kingdom, United States
Collaborators--

Timeline

N/ACompletedFinished
19961997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedNov 4, 1999
Enrollment StartMay 22, 1996
Primary CompletionNov 13, 2009
TodayJul 2, 2026
Enrollment to primary: 13.5 yearsPosted 26.7 years ago