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Therapeutic Benefit of Incobotulinum Toxin A for Spasticity of the Triceps Surae in Patients With Multiple Sclerosis (GAITOX)

P

Pôle Saint Hélier

Status

Completed

Conditions

Multiple Sclerosis

Treatments

Drug: Incobotulinum toxin A

Study type

Observational

Funder types

Other

Identifiers

NCT04265092
Pole-sthelier

Details and patient eligibility

About

Introduction/Objectives: In this observational study, we assessed the benefit following an injection of 200 international units (IU) of incobotulinum toxinA in patients with multiple sclerosis (MS) with spasticity of the triceps surae (TS) at 6 weeks (peak efficacy of toxin) and at 3 months (cancellation of efficacy).

Methods: This study enrolled all MS patients willing to participate with Expanded Disability Status Scale (EDSS) scores of less than 6, who required toxin for management of focal spasticity of the TS. Treatment consisted of 200 IU of incobotulinum toxinA injected into the TS. Outcome measures were assessed before injection, at 6 weeks and 3 months post-injection, using the Goal Attainment Scale (GAS), Twelve Item MS Walking (MSWS-12) Scale, Timed Up and Go (TUG) Test, 6 Minute Walk Test (6MWT). Spatiotemporal gait data was obtained by GAITRite.

Enrollment

22 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • MS patients aged over 18 years
  • with gait problems related to spasticity of the triceps surae,
  • walking 10 m in less than a minute,
  • with or without technical assistance,
  • with an EDSS of 6.5 or less
  • triceps surae spasticity of between 1 and 3 on the Modified Ashworth Scale.

Exclusion criteria

  • Comprehension problems preventing the patient from expressing his/her free and informed consent to the study.
  • Intolerance to botulinum toxin;
  • botulinum toxin injection in the previous three months.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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