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ClinicalTrials.gov record
Completed No phase listed Observational

Effectiveness and Safety of Dysport® (abobotulinumtoxinA) in Paediatric Lower Limb Spasticity

ClinicalTrials.gov ID: NCT03017729

Public ClinicalTrials.gov record NCT03017729. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 8:13 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase IV, Prospective, Observational, Multicentre Study Evaluating the Effectiveness and Safety of Dysport® (abobotulinumtoxinA) in Paediatric Lower Limb Spasticity.

Study identification

NCT ID
NCT03017729
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Ipsen
Industry
Enrollment
242 participants

Conditions and interventions

Interventions

  • Botulinum toxin type A Biological

Biological

Eligibility (public fields only)

Age range
2 Years to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 9, 2017
Primary completion
Nov 29, 2020
Completion
Nov 29, 2020
Last update posted
Dec 18, 2020

2017 – 2020

United States locations

U.S. sites
27
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Children's National Medical Center Washington D.C. District of Columbia 20010
Nicklaus Children's Hospital Miami Florida 33155
Laszlo J. Mate, M.D. North Palm Beach Florida 33408
Clinical Integrative Research Central Atlanta Atlanta Georgia 30328
Mt. Washington Pediatric Hospital Baltimore Maryland 21209
William Beaumont Hospital Pediatric Research Royal Oak Michigan 48073
Gillette Children's Specialty Healthcare Saint Paul Minnesota 55101
University of Missouri Columbia Missouri 65212
Washington University School Of Medicine St Louis Missouri 63110
Valley Health System Ridgewood New Jersey 07450
Montefiore Medical Center The Bronx New York 10467
Akron Children's Hospital Akron Ohio 44308
Cleveland Clinic Cleveland Ohio 44195
Dayton Children's Hospital Dayton Ohio 45404
The Children's Center Bethany Oklahoma 73008
Shriners Hospitals for Children Portland Oregon 97239
Good Shepherd Rehabilitation Network Allentown Pennsylvania 18103
Shriners Hospitals for Children Philadelphia Pennsylvania 19140
Shriners Hospitals for Children Greenville South Carolina 29605
Children's Hospital at Erlanger Chattanooga Tennessee 37403
Scottish Rite Hospital for Children Dallas Texas 75219
Shriners Hospitals for Children Houston Texas 77030
Texas Children's Hospital Houston Texas 77030
Texas Children's Plano Texas 75024
The Children's Hospital of San Antonio San Antonio Texas 78207
Utah Neuro Rehabilitation Murray Utah 84124
Children's Hospital of Wisconsin Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03017729, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 18, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03017729 live on ClinicalTrials.gov.

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