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To Document the Effectiveness of BoNT-A Injection in Adult Subjects With Upper Limb Spasticity Following Stroke | Clinical Trials | Clareo Health

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To Document the Effectiveness of BoNT-A Injection in Adult Subjects With Upper Limb Spasticity Following Stroke

An International, Prospective Cohort to Document the Effectiveness of One BoNT-A Injection Cycle Based on Attainment of Individual Person-centred Goals in Adult Subjects Suffering From Upper Limb Spasticity Following Stroke

NCT01020500•Ipsen

View on ClinicalTrials.gov

Summary

The purpose of the study is to assess the responder rate as defined by the achievement of the primary goal from the Goal Attainment Scale following one BoNT-A injection cycle in accordance with routine practices.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Upper limb spasticity following stroke
•At least a 12-week interval between the last injection (BoNT-A or BoNT-B) and inclusion
•Decision already been agreed to inject BoNT-A
•Agreement with the subject on goal setting

Exclusion Criteria

•Contraindications to any BoNT-A preparations

Locations (96)

Rankin Park (site 036006)

Newcastle, Australia

Northshore Private Hospital (site 036003)

Sydney, Australia

Royal Prince Alfred Hospital (site 036005)

Sydney, Australia

Ryde Rehabilitation Center (site 036002)

Sydney, Australia

St Joseph's Hospital (site 036004)

Sydney, Australia

St Vincent's Hospital (site 036001)

Sydney, Australia

NÖ LKH Grimmenstein-Hochegg (site 040002)

Grimmenstein, Austria

Gaital-Kliniken Hermagor (site 040001)

Hermagor, Austria

Revalidatieziekenhuis Hof ter Schelde, August Vermeylenlaan 6 (site 056001)

Antwerp, Belgium

AZ St. Jan, Ruddershove 10, (site 056002)

Bruges, Belgium

Key Dates

Start Date

January 1, 2010

Primary Completion Date

May 1, 2011

Completion Date

May 1, 2011

Last Updated

November 6, 2020

Enrollment

469

ACTUAL participants

Conditions

Muscle Spasticity

Exoskeleton and Spinal Cord Stimulation for SCI

NCT03096197

Spinal Cord InjuryAmbulation Difficulty+1 more

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RECRUITINGNA

SIRS-ESWT Trial: Shoulder Internal Rotator Spasticity Trial Treated With Extracorporeal Shock Wave Therapy Trial

NCT06674785

StrokeMuscle Spasticity

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: November 6, 2020Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

To Document the Effectiveness of BoNT-A Injection in Adult Subjects With Upper Limb Spasticity Following Stroke

Inclusion Criteria

Exclusion Criteria

Exoskeleton and Spinal Cord Stimulation for SCI

SIRS-ESWT Trial: Shoulder Internal Rotator Spasticity Trial Treated With Extracorporeal Shock Wave Therapy Trial

"Comparison of Therapist-Led and Robot-Assisted Arm Therapy in Subacute Stroke Rehabilitation"

A Study to Collect Participants Experience of Living With Adult Upper Limb (AUL) Spasticity and to Assess the Arm Activity Measure (ArmA)

Measurements of Displacement Amplitude and Angular Velocities During Passive Extension of the Wrist and Hand Complex in Stroke Patients

Muscle Selection for Botulinum Toxin A Injection in Poststroke Elbow Flexor Spasticity