Clinical Trials Directory

Trials / Unknown

UnknownNCT01664013

The Impact of Botulinum Toxin Treatment in Quality of Life of Cervical Dystonia Patients

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Roongroj Bhidayasiri · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate the impact of botulinum toxin treatment in quality of life(QoL) in cervical dystonia patients

Conditions

Interventions

TypeNameDescription
DRUGNuronoxReconstituted Neuronox® is injected at a dose determined by the physician based upon his/her clinical experience with botulinum toxin.Actual dose and injection site should be adjusted individually considering the muscle mass, degree of spasticity, body weight, and response to any previous botulinum toxin injections.

Timeline

Start date
2012-10-01
Primary completion
2013-10-01
First posted
2012-08-14
Last updated
2013-08-20

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT01664013. Inclusion in this directory is not an endorsement.