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Clinical Trial Summary

Osteoporosis pseudoglioma (OPPG) syndrome is a rare autosomal recessive condition of childhood osteoporosis and congenital blindness for which new treatments are needed. We have found that body fat is increased in OPPG and muscle mass is reduced. We hypothesize that growth hormone therapy will improve muscle mass and bone strength in OPPG.


Clinical Trial Description

Osteoporosis pseudoglioma (OPPG) syndrome is a rare autosomal recessive condition of childhood osteoporosis and congenital blindness for which new treatments are needed. We have found that body fat is increased in OPPG and muscle mass is reduced. We hypothesize that growth hormone therapy will improve muscle mass and bone strength in OPPG. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01614171
Study type Interventional
Source University of Maryland, Baltimore
Contact
Status Withdrawn
Phase N/A
Start date December 2013
Completion date December 2015