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Spasticity and Treatment Satisfaction Among Stroke Survivors

NCT03995524 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2020-06-01

No results posted yet for this study

Summary

To investigate, through ethnography, changes in symptom burden and disability and their effects/interference on patient functioning, ability to perform activities of daily living (ADL) and quality of life (QoL) throughout the duration of one BoNT-A treatment cycle.

Conditions

  • Spasticity as Sequela of Stroke

Sponsors & Collaborators

Principal Investigators

  • Ipsen Medical Director · Ipsen

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-07-20
Primary Completion
2020-05-12
Completion
2020-05-12

Countries

  • France

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03995524 on ClinicalTrials.gov