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NCT04908423RecruitingPhase 4

Xeomin® and Gait Related Mobility After Stroke

Upper Extremity Injection of Xeomin® and Changes in Gait Related Mobility in Adults After Stroke

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

The aim of the present pilot study is to evaluate the association between change in gait related mobility in ambulatory male and female adult hemiparetic patients before and 4-6-weeks after Xeomin® injection into the upper limb, using two standardized tests of physical function in outpatient rehabilitation that are widely used; the 10-meter walk test and the timed 'up and go' test (TUG).

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
20 (estimated)
First submitted
25 May 2021
Start date
19 Oct 2021
Primary completion date
Apr 2028
Lead sponsor
Wake Forest University Health Sciences
Diseases
Stroke
NCT number
NCT04908423

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 20
  • From 19 Oct 2021 to the primary completion date, Apr 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Weight bearing restrictions due to concurrent orthopedic injuries that would make ambulating with or without an assistive device unsafe

Other illness

  • Participants with uncorrected hearing impairment
  • Other confounding neurological diagnoses or active acute illness (cancer, Parkinson's disease, multiple sclerosis)

Other

  • Passive range of motion at either the ankle, knee, or elbow joint less than 30 degrees
  • Speech language expression deficit (e.g., aphasia)
  • Absence of proprioception upon neurologic examination
  • Presence of fixed contractures in the upper or lower extremities not correctable to neutral

Who the study is looking for

  • Diagnosis of hemiparesis and spasticity secondary to stroke with upper and lower limb spasticity and unilateral motor and/or sensory deficit
  • No prior surgery to the lower limb
  • Able to walk at least 10 meters without physical assistance from another person and without an assistive device
  • Toe- ground clearance during swing phase without assistive device or orthoses
  • No treatment with botulinum toxin within the past 4 months

Age in the registry: 18 years to 79 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Carolinas Rehabilitation
Coordinator of this site? Confirm its status
CharlotteUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.