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Clinical Trial Summary

Botulinum neurotoxin (BoNT) is injected into muscles for treatment of dystonia. BoNTs are zinc proteases, and their enzymatic effect is reduced in the setting of low zinc. The study hypothesis is that a large enough fraction of unselected dystonia patients receiving BoNT injection have suboptimal zinc concentration in their tissues, and will experience improved response to BoNT if the injection is preceded by oral zinc supplementation (OZS). OZS consists of 50 mg of zinc acetate oral tablet each day for 7 days before injection. This is a double blind placebo controlled cross-over study, randomized order placebo and OZS, in patients at a neurology clinic on stable dose of BoNT.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05095493
Study type Interventional
Source University of Texas Southwestern Medical Center
Contact
Status Completed
Phase N/A
Start date January 1, 2013
Completion date October 31, 2014

See also
  Status Clinical Trial Phase
Recruiting NCT03428009 - Dystonia Genotype-Phenotype Correlation
Recruiting NCT04560101 - Motor and Non-motor Symptoms in Cervical Dystonia