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Study of Pituitary Size and Function in Familial Dwarfism of Sindh
This study has been completed.
Study NCT00004365   Information provided by Office of Rare Diseases (ORD)
First Received: October 18, 1999   Last Updated: June 23, 2005   History of Changes

October 18, 1999
June 23, 2005
September 1995
 
 
 
Complete list of historical versions of study NCT00004365 on ClinicalTrials.gov Archive Site
 
 
 
Study of Pituitary Size and Function in Familial Dwarfism of Sindh
 

OBJECTIVES: I. Assess pituitary size and anatomic configuration by magnetic resonance imaging (MRI) in 4 affected dwarfs in the province of Sindh, Pakistan.

II. Evaluate ultradian growth hormone (GH) secretory patterns in 4 affected dwarfs.

PROTOCOL OUTLINE: Pituitary size and anatomy and growth hormone response are evaluated.

All patients undergo MRI of the pituitary fossa on day 1. On day 2, homozygous patients receive a slow infusion of normal saline with blood sampling every 10 minutes.

 
Observational
Screening
Growth Hormone Deficiency
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
4
February 2000
 
  • Familial Dwarfism of Sindh
  • Severe short stature but proportionate without dysmorphic features
  • Normal body size and weight at birth
  • Bone age is severely delayed
  • Puberty is somewhat delayed (age 15-16)
  • Fertility present in at least 3 dwarfs
Both
10 Years to 60 Years
No
Contact information is only displayed when the study is recruiting subjects
 
 
NCT00004365
 
199/11940, NU-571
National Center for Research Resources (NCRR)
Northwestern University
Study Chair: Gerhard Baumann Northwestern University
Office of Rare Diseases (ORD)
December 2003

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