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NF2 Natural History Consortium
This study is ongoing, but not recruiting participants.
Study NCT00004483   Information provided by Office of Rare Diseases (ORD)
First Received: October 18, 1999   Last Updated: September 27, 2005   History of Changes

October 18, 1999
September 27, 2005
January 2002
 
 
 
Complete list of historical versions of study NCT00004483 on ClinicalTrials.gov Archive Site
 
 
 
NF2 Natural History Consortium
 

OBJECTIVES:

I. Define the growth rates and clinical course of NF2-related tumors in patients with neurofibromatosis type 2. Associate growth rate with physical function.

PROTOCOL OUTLINE: Data on the clinical course and growth rate of NF2-related tumors in patients with neurofibromatosis 2. Patients are evaluated each year on a cranial and a spinal MRI, eye tests, hearing tests, quality of life, neurological tests, and physical functioning.

 
Observational
Natural History, Longitudinal
  • Schwannoma, Vestibular
  • Neurofibromatosis 2
  • Meningioma
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
100
 
 

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

  • Diagnosed with neurofibromatosis 2 on or after 01/01/93
  • Must meet one of the following conditions:

Bilateral vestibular schwannoma OR Family history of neurofibromatosis 2 (first degree family relative) AND Unilateral vestibular schwannoma at under 30 years OR Any 2 of the following: Meningioma Glioma Schwannoma Juvenile posterior subcapsular lenticular opacity/juvenile cortical cataract

  • No plans to treat vestibular schwannoma in next 12 months

--Prior/Concurrent Therapy--

  • Not specified

--Patient Characteristics--

  • Age: 5 and over
Both
5 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00004483
 
199/14226, HEI-NF2, HEI-DAMD17-01-1-0710
House Ear Institute
 
Study Chair: William H. Slattery, III House Ear Institute
Office of Rare Diseases (ORD)
September 2005

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