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Clinical Trial Summary

The aim of this study is to perform, in real world clinical practice, a three-dimensional assessment from patient's, caregiver's and physician's perspectives, of the impact of AboBoNT-A on caregiver burden, functional disability and other health care measures in patients affected with ULS due to acquired brain injuries.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06245772
Study type Observational
Source Ipsen
Contact Ipsen Clinical Study Enquiries
Phone See e mail
Email clinical.trials@ipsen.com
Status Recruiting
Phase
Start date November 16, 2023
Completion date January 16, 2026

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