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Completed

NCT Number: NCT01935544

Effectiveness of Two Techniques in Injection Site Spotting for Botulinum Toxin Injections: Echography or Electro Stimulation.

Botulinum toxin injections are an effective treatment of limb spasticity after stroke. Different tracking techniques are used to locate a proper injection spot. Palpatory technique is barely effective and induces a high risk of error. Localization by electro stimulation is frequently used in adults, but often requires multiple painful repositioning of the needle. Ultrasound tracking is sometimes used in children but not much in adults.

The advantages of ultrasound-guided botulinum toxin injections are a painless localization and greater injection accuracy. Safety is therefore enhanced since intravascular injection is easily avoided.

The few existing publications on the subject are essentially case reports. Few studies have focused on comparing different injection techniques and so far, no well-conducted study has highlighted superior efficiency of ultrasound-guided injections.

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Key information

About this study

Objectives:

The main objective is to compare the efficiency of botulinum toxin injections depending on the localization technique: ultrasound vs. electrical stimulation.

The secondary objective is to demonstrate less painful localization associated to ultrasound-guidance.

Evaluations:

The primary endpoint is the variation of passive range of motion of ankle dorsiflexion at slow speed and high speed ("Tardieu scale") while keeping knee straight.

The secondary endpoints are:

  • The other components of the "Tardieu scale": quality of muscle reaction (X) at slow speed and fast speed, angle of apparition of the muscle reaction (Y) at slow speed and fast speed.
  • Assessment of spasticity of the triceps surae on the modified Ashworth scale.
  • The walking speed.
  • The extent of pain at the injection site by visual analogue scale.
  • The duration of tracking and injection.

Methodology:

This prospective, randomized, single-center, single-blind, cross-over, study will be conducted in chronic stroke patients with spasticity of the triceps surae.

Patients will receive two injections during the protocol, each with a different technique of localization. Randomization will determine which technique will be used in the first and the second place.

Patients will be selected from the cohort of patients supported by consultation of Physical Medicine and Rehabilitation Department of the University Hospital of Clermont-Ferrand. Injections of botulinum toxin and assessments will take place in the same department.

The study period is five months for each patient. This study does not present a major risk for the subjects. The main inconvenience is injection pain or side effects of botulinum toxin (increase of motor deficits or dysphagia).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 to 80 years.
  • Hemiplegia sequelae of stroke
  • Spasticity of the triceps surae listed at least 1 + / 4 on the modified Ashworth scale
  • Ability to give written consent

Exclusion criteria

  • Injection of botulinum toxin older than 3 months
  • Patient who has already received ultrasound-guided injection of botulinum toxin
  • Indication of botulinum toxin injection in other muscle groups in the lower limb than triceps surae
  • Swallowing impairment
  • Ongoing AVK anticoagulation treatment with INR greater than 3 during one week before randomization.
  • Ongoing treatment by aminoglycosides
  • General anesthesia with injection of curare planned during the participation in the protocol
  • Wearing a pacemaker
  • History of ankle arthrodesis
  • Other cons-indication for botulinum toxin injection: myasthenia gravis, pregnancy, lactation.

Treatment and study plan

Botulinum toxin injection

Device

Primary outcomes

  1. Passive range of motion of ankle dorsiflexion (Tardieu scale) while keeping knee straight

    Time frame: at inclusion

  2. Passive range of motion of ankle dorsiflexion (Tardieu scale) while keeping knee straight

    Time frame: at day 1 (first injection)

  3. Passive range of motion of ankle dorsiflexion (Tardieu scale) while keeping knee straight

    Time frame: at day 60

  4. Passive range of motion of ankle dorsiflexion (Tardieu scale) while keeping knee straight

    Time frame: at day 120 (second injection)

  5. Passive range of motion of ankle dorsiflexion (Tardieu scale) while keeping knee straight

    Time frame: at day 150

Secondary outcomes

  1. Tardieu scale: quality of muscle reaction at slow speed and fast speed

    Time frame: at Inclusion, D1, D60, D120 and D150

  2. Angle of apparition of the muscle reaction at slow speed and fast speed

    Time frame: at Inclusion, D1, D60, D120 and D150

  3. Spasticity of the triceps surae on the modified Ashworth scale

    Time frame: at Inclusion, D1, D60, D120 and D150

  4. Walking speed

    Time frame: at Inclusion, D1, D60, D120 and D150

  5. Extent of pain at the injection site by visual analogue scale

    Time frame: at D1, D120

  6. Duration of tracking and injection

    Time frame: at D1, D120

Sponsors and collaborators

Lead sponsor

University Hospital, Clermont-Ferrand

Other

Registry information

Important dates

Study start
2013
Primary completion
2019
Study completion
2019
First posted
Sep 5, 2013
Registry last updated
Oct 9, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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