Status:
COMPLETED
Treatment With Xeomin Versus Botox in Children With Spastic Equine and Equinovarus Foot Deformation in Pediatric Cerebral Palsy
Lead Sponsor:
Merz Pharmaceuticals GmbH
Collaborating Sponsors:
LLC Merz Pharma, Russia
Conditions:
Cerebral Palsy
Spastic Paraplegia and Hemiparesis
Eligibility:
All Genders
2-12 years
Phase:
PHASE2
Brief Summary
1. To assess the clinical and neurophysiological efficacy of Xeomin® vs. Botox® in children with spastic equine and equinovarus foot deformation in pediatric cerebral palsy 2. To assess the safety of ...
Eligibility Criteria
Inclusion
- Children from 2 through 12 years of age, of both sexes, suffering from spastic paraplegia or hemiparesis in pediatric cerebral palsy.
- Equine and equinovarus foot posture.
- Gastrocnemius spasticity of 2 points and greater, by modified Ashworth scale.
- Patient can walk unassisted or with a support.
- Mental development of patients is normal or mildly retarded.
- Previous course of spasticity treatment with BTA products was completed earlier than at 6 months before this trial or never administered before.
- Patient's parents have signed an informed consent, are able and wishing to adhere to procedures described in the trial protocol and to the schedule of visits throughout the entire period of treatment.
Exclusion
- Fixed ankle joint contracture.
- Previous denervation of spastic muscles by surgery, phenol or alcohol;
- Athetosis and dystonia in the area of injected muscles.
- Inflammation at the planned injection site.
- Elevated body temperature and acute (infectious and non-infectious) diseases at the time of injection.
- Neuromuscular transmission disorders (myasthenia gravis, Lambert-Eaton syndrome, etc.).
- Decompensated physical diseases potentially affecting the trial findings.
- Acute fever, infection or surgery within 1 month before the trial.
- Use of aminoglycosides or spectinomycin within 1 month before starting the trial.
- Hypersensitivity to any of product ingredients.
- Positive history for allergies (especially with regard to protein-containing products).
- Patient's parents are unable or unwilling to adhere to the trial protocol requirements including signing the informed consent and conforming to the schedule of visits.
- Participation in other clinical trials in the last 4 weeks before inclusion.
Key Trial Info
Start Date :
July 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2016
Estimated Enrollment :
64 Patients enrolled
Trial Details
Trial ID
NCT02188277
Start Date
July 1 2014
End Date
December 1 2016
Last Update
January 26 2017
Active Locations (3)
Enter a location and click search to find clinical trials sorted by distance.
1
State Budget Institution of Health in Moscow "Scientific and Practical Center of Pediatric psychoneurology Moscow Health Department"
Moscow, Russia, 119602
2
Federal State Autonomous Institution "Scientific Center of Children's Health" of the Ministry of Health of the Russian Federation
Moscow, Russia, 119991
3
Federal State Budget Educational Institution of Higher Professional Learning "Stavropol State Medical University" of the Ministry of Health of the Russian Federation
Stavropol, Russia, 355017